FIRST FOOD

Main information

  • Trade name:
  • FIRST FOOD 400G
  • Composition:
  • 400G
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • FIRST FOOD 400G
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

18-4-2018

The impact of global change on the emergence of plant diseases and pests in Europe

The impact of global change on the emergence of plant diseases and pests in Europe

The French Agency for Food, Environmental and Occupational Health and Safety (ANSES), in collaboration with the European Food Safety Authority (EFSA) and the European and Mediterranean Plant Protection Organization (EPPO), is organising a conference on 23-24 April 2018 in Paris. This two-day event will review the current state of scientific knowledge worldwide and provide a forum for sharing experiences on the reasons for the emergence of plant diseases and pests, as well as their impact on the environme...

France - Agence Nationale du Médicament Vétérinaire

18-4-2018

Carnivore Meat Company Issues Voluntary Recall of limited batches of “Vital Essentials® Freeze-Dried Beef Toppers” and “Vital Essentials® Frozen Beef Chub Entrée for Dogs” Pet Food

Carnivore Meat Company Issues Voluntary Recall of limited batches of “Vital Essentials® Freeze-Dried Beef Toppers” and “Vital Essentials® Frozen Beef Chub Entrée for Dogs” Pet Food

Carnivore Meat Company of Green Bay, WI, is voluntarily recalling a limited amount of pet food because the products may have the potential to be contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

17-4-2018

FDA approves first therapy for rare inherited form of rickets, x-linked hypophosphatemia

FDA approves first therapy for rare inherited form of rickets, x-linked hypophosphatemia

FDA approved Crysvita (burosumab), the first drug approved to treat adults and children ages 1 year and older with x-linked hypophosphatemia (XLH), a rare form of rickets.

FDA - U.S. Food and Drug Administration

17-4-2018

Statement by Dr. Susan Mayne on FDA efforts to reduce consumer exposure to arsenic in rice

Statement by Dr. Susan Mayne on FDA efforts to reduce consumer exposure to arsenic in rice

One way FDA oversees food safety is through monitoring of contaminants in food, such as arsenic, assessing potential exposure and taking steps to reduce exposure

FDA - U.S. Food and Drug Administration

16-4-2018

Vitakraft Sun Seed Recalls of Sunseed Vita Prima Sugar Glider Food Due to Possible <em>Salmonella</em> Health Risk

Vitakraft Sun Seed Recalls of Sunseed Vita Prima Sugar Glider Food Due to Possible <em>Salmonella</em> Health Risk

Vitakraft Sun Seed Inc. of Weston, OH, is voluntarily recalling one lot of Sunseed Vita Prima Exotics Sugar Glider Formula because it has the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

FDA - U.S. Food and Drug Administration

15-4-2018

K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible <em>Listeria Monocytogenes</em>

K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible <em>Listeria Monocytogenes</em>

K9 Natural Ltd is voluntarily recalling four batches of the K9 Natural Frozen Chicken Feast 2.2lb and 11lb bags that was imported into the US market in June 2017 because they have the potential to be contaminated with Listeria Monocytogenes.

FDA - U.S. Food and Drug Administration

14-4-2018

Urgent: Voluntary Product Recall of Vuse Vibe Power Units

Urgent: Voluntary Product Recall of Vuse Vibe Power Units

R.J. Reynolds Vapor Company has voluntarily initiated a nationwide safety recall of all Vuse Vibe power units. The Company initiated the recall after receiving consumer complaints about malfunctioning batteries, which may cause the power unit to overheat and create a fire risk. The Company notified the U.S. Food and Drug Administration regarding the issue and will be working directly with the Agency on this voluntary recall.

FDA - U.S. Food and Drug Administration

13-4-2018

FDA takes step to protect consumers against dietary supplements containing dangerously high levels of extremely concentrated or pure caffeine

FDA takes step to protect consumers against dietary supplements containing dangerously high levels of extremely concentrated or pure caffeine

Today, the U.S. Food and Drug Administration took an important step to better protect consumers from the dangers of highly concentrated and pure caffeine products.

FDA - U.S. Food and Drug Administration

13-4-2018

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group, Inc., of Miami, FL, is voluntarily recalling its ten-ounce packages of La Marinera Brand Dried Yellow Potatoes because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

11-4-2018

FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems

FDA permits marketing of artificial intelligence-based device to detect certain diabetes-related eye problems

FDA permits marketing of first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.

FDA - U.S. Food and Drug Administration

11-4-2018

ANSES recommends that certain populations avoid the consumption of food supplements containing melatonin

ANSES recommends that certain populations avoid the consumption of food supplements containing melatonin

Under the national nutrivigilance scheme, reports of adverse effects likely to be associated with the consumption of food supplements containing melatonin have been brought to the attention of ANSES. A retrospective analysis of these reports, combined with the considerable level of consumption of this type of supplement, led ANSES to conduct an assessment of the potential health risks.

France - Agence Nationale du Médicament Vétérinaire

10-4-2018

FDA clears first contact lens with light-adaptive technology

FDA clears first contact lens with light-adaptive technology

FDA clears first contact lens with additive that automatically darkens the lens when exposed to bright light

FDA - U.S. Food and Drug Administration

6-4-2018

Aspire Food Group Issues Alert on Undeclared Sulfites in Exo Bars

Aspire Food Group Issues Alert on Undeclared Sulfites in Exo Bars

Aspire Food Group of Austin, TX, is recalling its 60 gram bars of EXO Blueberry Vanilla, Peanut Butter & Jelly, and Apple Cinnamon bars because they may contain undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reaction if they consume these products.

FDA - U.S. Food and Drug Administration

5-4-2018

Exposure to silver nanoparticles

Exposure to silver nanoparticles

Silver nanoparticles are used in various industrial applications, in sectors such as food (additives, food packaging, internal linings of refrigerators), textiles (clothing and bedding) and cosmetic and hygiene products (toothbrushes, hair straighteners, disinfectant sprays, etc.). They are mainly used for their antibacterial and antifungal properties. However, it is still proving very difficult to obtain an inventory referencing all products containing silver nanoparticles in France and elsewhere in the...

France - Agence Nationale du Médicament Vétérinaire

3-4-2018

FDA Orders Mandatory Recall for Kratom Products Due to Risk of <em>Salmonella</em>

FDA Orders Mandatory Recall for Kratom Products Due to Risk of <em>Salmonella</em>

Today, the U.S. Food and Drug Administration announced it has issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall. This is the first time the agency has issued a mandatory recall order to protect Americans from contaminated food products.

FDA - U.S. Food and Drug Administration

3-4-2018

FDA orders mandatory recall for kratom products due to risk of salmonella

FDA orders mandatory recall for kratom products due to risk of salmonella

Today, the U.S. Food and Drug Administration announced it has issued a mandatory recall order for all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC, after several were found to contain salmonella. The agency took this action after the company failed to cooperate with the FDA’s request to conduct a voluntary recall. This is the first time the agency has issued a mandatory recall order to protect Americans from contaminated food products.

FDA - U.S. Food and Drug Administration

2-4-2018

New York raw milk cheese company ordered to stop sales for food safety violations

New York raw milk cheese company ordered to stop sales for food safety violations

FDA announces an enforcement action taken against Vulto Creamery of New York. The company cannot sell ready-to-eat raw cheese product until it complies with the consent decree. Vulto was linked to an outbreak last year.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Black Lion Pill contains hidden drug ingredient

Public Notification: Black Lion Pill contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Black Lion Pill, a product promoted and sold for sexual enhancement on various websites, including www.rakuten.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Rhino 69 Extreme 50000 contains hidden drug ingredient

Public Notification: Rhino 69 Extreme 50000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Rhino 69 Extreme 50000, a product promoted and sold for sexual enhancement on various websites, including www.bonanza.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Public Notification: Red Zone Xtreme 3000 contains hidden drug ingredient

Public Notification: Red Zone Xtreme 3000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Red Zone Xtreme 3000, a product promoted and sold for sexual enhancement on various websites, including www.ebay.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

28-3-2018

Foot-and-mouth disease: a new international reference mandate for ANSES

Foot-and-mouth disease: a new international reference mandate for ANSES

Through its Maisons-Alfort Laboratory for Animal Health, ANSES has just been appointed Reference Centre of the Food and Agriculture Organisation of the United Nations (FAO) for foot-and-mouth disease and vesicular diseases. This new mandate expands the reference activities of the Maisons-Alfort Laboratory for Animal Health regarding foot-and-mouth disease, particularly in the context of its reference mandates at a national, European and international level, and is recognition of ANSES's commitment to add...

France - Agence Nationale du Médicament Vétérinaire

28-3-2018

First Source Issues Allergy Alert on Undeclared Peanuts in Wegmans 9 Oz Yogurt Raisins

First Source Issues Allergy Alert on Undeclared Peanuts in Wegmans 9 Oz Yogurt Raisins

First Source of Tonawanda, NY, is voluntarily recalling 9 OZ packages of Wegmans Yogurt Raisins, because the product may contain undeclared peanuts. People who have an allergy or sensitivity to peanuts run the risk of serious or life- threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

27-3-2018

FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices

FDA authorizes first fully interoperable continuous glucose monitoring system, streamlines review pathway for similar devices

The authorization classifies integrated continuous glucose monitoring devices in class II and subjects them to certain criteria called special controls

FDA - U.S. Food and Drug Administration

26-3-2018

Blue Ridge Beef Voluntarily Recalls BRB Complete Raw Pet Food Lot#GA0131 Because of Possible Contamination

Blue Ridge Beef Voluntarily Recalls BRB Complete Raw Pet Food Lot#GA0131 Because of Possible Contamination

Blue Ridge Beef of Eatonton, GA, is voluntarily recalling lot#GA0131 of BRB Complete raw pet food because of the potential of contamination with Salmonella and Listeria monocytogenes. The cause of the recall: This recall was initiated after samples collected and tested by the FDA showed positive for Salmonella and Listeria monocytogenes. There has been no consumer or pet illnesses in association with this product. Blue Ridge Beef is voluntarily recalling this product lot as a commitment to consumer and p...

FDA - U.S. Food and Drug Administration

26-3-2018

Mrs. Gerry’s Kitchen Issues Allergen Alert on Undeclared Seafood in Salad

Mrs. Gerry’s Kitchen Issues Allergen Alert on Undeclared Seafood in Salad

The salads may contain undeclared traces of imitation crab meat. People who have allergies to fish or shell fish run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled salad was shipped to retail and food service distributers in IL, IA, KS, MI, MN, MT, NE, ND, SD, UT, and WI. No illnesses have been reported to date in connection with this problem.

FDA - U.S. Food and Drug Administration

21-3-2018

5 Things to Know About Breast Implants

5 Things to Know About Breast Implants

The U.S. Food and Drug Administration regulates breast implants as medical devices. Learn about the risks of these products, and consider this advice.

FDA - U.S. Food and Drug Administration

20-3-2018

Radagast Pet Food, Inc. Voluntarily Recalls One Lot of Rad Cat Raw Diet Free-Range Chicken and One Lot of Free-Range Turkey Recipe Because of Possible Health Risk

Radagast Pet Food, Inc. Voluntarily Recalls One Lot of Rad Cat Raw Diet Free-Range Chicken and One Lot of Free-Range Turkey Recipe Because of Possible Health Risk

Radagast Pet Food, Inc. of Portland, OR is recalling one lot of Free-Range Chicken and one lot of Free-Range Turkey Recipe because they have the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

FDA - U.S. Food and Drug Administration

20-3-2018

FDA expands approval of Adcetris for first-line treatment of Stage III or IV classical Hodgkin lymphoma in combination with chemotherapy

FDA expands approval of Adcetris for first-line treatment of Stage III or IV classical Hodgkin lymphoma in combination with chemotherapy

FDA approves Adcetris (brentuximab vedotin) to treat adult patients with previously untreated stage III or IV classical Hodgkin lymphoma (cHL) in combination with chemotherapy

FDA - U.S. Food and Drug Administration

16-4-2018

FDA Takes Steps Against Dietary Supplements Containing Dangerously High Levels of Pure Caffeine

FDA Takes Steps Against Dietary Supplements Containing Dangerously High Levels of Pure Caffeine

Today, the U.S. Food and Drug Administration took an important step to better protect consumers from the dangers of highly concentrated and pure caffeine products. These products present a significant public health threat because of the high risk that they will be erroneously used at excessive, potentially dangerous doses. Highly concentrated and pure caffeine, often sold in bulk packages, have been linked to at least two deaths in otherwise healthy individuals.

US - RxList

16-4-2018

Provisional approval pathway - first determination decision

Provisional approval pathway - first determination decision

First medicine to be granted a provisional approval determination

Therapeutic Goods Administration - Australia

14-4-2018

Doctors Curbing First-Time Prescriptions for Opioids

Doctors Curbing First-Time Prescriptions for Opioids

Title: Doctors Curbing First-Time Prescriptions for OpioidsCategory: Health NewsCreated: 4/12/2018 12:00:00 AMLast Editorial Review: 4/13/2018 12:00:00 AM

US - MedicineNet

12-4-2018

First Auto-Darken Contact Lenses Approved

First Auto-Darken Contact Lenses Approved

Title: First Auto-Darken Contact Lenses ApprovedCategory: Health NewsCreated: 4/10/2018 12:00:00 AMLast Editorial Review: 4/11/2018 12:00:00 AM

US - MedicineNet

12-4-2018

FDA OKs AI Device to Detect Diabetic Retinopathy

FDA OKs AI Device to Detect Diabetic Retinopathy

The FDA has approved the first medical device that uses artificial intelligence (AI) software to detect diabetic retinopathy in adults with diabetes that can be used by non-eye care professionals.

US - RxList

11-4-2018

#ICYMI FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.  http://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #Me

#ICYMI FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. http://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #Me

#ICYMI FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. http://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalDevice pic.twitter.com/kpQyicVEWM

FDA - U.S. Food and Drug Administration

11-4-2018

FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes.  https://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalD

FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. https://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalD

FDA permits marketing of the first medical device to use artificial intelligence to detect greater than a mild level of diabetic retinopathy in the eye of adults who have diabetes. https://go.usa.gov/xQTE2  #Diabetes #ArtificialIntelligence #AI #MedicalDevice

FDA - U.S. Food and Drug Administration

11-4-2018

FDA OKs First Transitional Contacts That Darken in Sunlight

FDA OKs First Transitional Contacts That Darken in Sunlight

The first contact lenses that have an additive that automatically darkens the lenses when exposed to bright light have been cleared by the US Food and Drug Administration (FDA).

US - RxList

11-4-2018

First Transitional Contacts That Darken in the Sun

First Transitional Contacts That Darken in the Sun

FDA OKs First Transitional Contacts That Darken in Sunlight

US - eMedicineHealth

10-4-2018

England's Scarlet Fever Cases Highest in 36 Years

England's Scarlet Fever Cases Highest in 36 Years

An outbreak of scarlet fever in England and Wales has seen the highest number of cases reported in the first quarter of a year since Public Health England (PHE) began collecting data in 1982.

US - RxList

6-4-2018

Scientific guideline:  Draft addendum to the guideline on the evaluation of medicinal products indicated for treatment of bacterial infections to address paediatric-specific clinical data requirements - First version, draft: consultation open

Scientific guideline: Draft addendum to the guideline on the evaluation of medicinal products indicated for treatment of bacterial infections to address paediatric-specific clinical data requirements - First version, draft: consultation open

This document proposes the development of an addendum to the Guideline on the evaluation of medicines indicated for treatment of bacterial infections CPMP/EWP/558/95 rev 2), to provide specific guidance on paediatric clinical development programmes to support the authorisation of antibacterial agents for treating infectious diseases in children.

Europe - EMA - European Medicines Agency

3-4-2018

FDA to Move Ahead With Obama Administration Food Labeling Rules

FDA to Move Ahead With Obama Administration Food Labeling Rules

Title: FDA to Move Ahead With Obama Administration Food Labeling RulesCategory: Health NewsCreated: 3/30/2018 12:00:00 AMLast Editorial Review: 4/2/2018 12:00:00 AM

US - MedicineNet

3-4-2018

Health Tip: Keep Pet Food Safe

Health Tip: Keep Pet Food Safe

Title: Health Tip: Keep Pet Food SafeCategory: Health NewsCreated: 4/2/2018 12:00:00 AMLast Editorial Review: 4/2/2018 12:00:00 AM

US - MedicineNet

2-4-2018

CALAMINE (Ferric Oxide Red) Lotion [Wakefern Food Corp]

CALAMINE (Ferric Oxide Red) Lotion [Wakefern Food Corp]

Updated Date: Apr 2, 2018 EST

US - DailyMed

2-4-2018

LAXATIVE GENTLE (Bisacodyl) Tablet, Sugar Coated [SAVE-A-LOT FOOD STORES, LTD.]

LAXATIVE GENTLE (Bisacodyl) Tablet, Sugar Coated [SAVE-A-LOT FOOD STORES, LTD.]

Updated Date: Apr 2, 2018 EST

US - DailyMed

2-4-2018

DRY SCALP CARE (Pyrithione Zinc) Shampoo [Wakefern Food Corp]

DRY SCALP CARE (Pyrithione Zinc) Shampoo [Wakefern Food Corp]

Updated Date: Apr 2, 2018 EST

US - DailyMed

31-3-2018

Unhealthy Phthalate Chemicals Found in Restaurant Food

Unhealthy Phthalate Chemicals Found in Restaurant Food

Title: Unhealthy Phthalate Chemicals Found in Restaurant FoodCategory: Health NewsCreated: 3/29/2018 12:00:00 AMLast Editorial Review: 3/30/2018 12:00:00 AM

US - MedicineNet

29-3-2018

Michelle Tarver, MD, PhD. - Ophthalmologist and Epidemiologist here at the FDA’s Center for Devices and Radiological Health,  organized the first Patient Engagement Advisory Committee (PEAC) Meeting as Acting Assistant Director of Strategic Programs, CDRH

Michelle Tarver, MD, PhD. - Ophthalmologist and Epidemiologist here at the FDA’s Center for Devices and Radiological Health, organized the first Patient Engagement Advisory Committee (PEAC) Meeting as Acting Assistant Director of Strategic Programs, CDRH

Michelle Tarver, MD, PhD. - Ophthalmologist and Epidemiologist here at the FDA’s Center for Devices and Radiological Health, organized the first Patient Engagement Advisory Committee (PEAC) Meeting as Acting Assistant Director of Strategic Programs, CDRH #WomensHistoryMonth pic.twitter.com/ZlMfKbdayV

FDA - U.S. Food and Drug Administration

29-3-2018

FIRST AID ONLY ANTACID (Calcium Carbonate) Tablet, Chewable [Acme United Corporation]

FIRST AID ONLY ANTACID (Calcium Carbonate) Tablet, Chewable [Acme United Corporation]

Updated Date: Mar 29, 2018 EST

US - DailyMed

28-3-2018

Sports 'Sponsorships' Hawk Junk Food to Kids

Sports 'Sponsorships' Hawk Junk Food to Kids

Title: Sports 'Sponsorships' Hawk Junk Food to KidsCategory: Health NewsCreated: 3/26/2018 12:00:00 AMLast Editorial Review: 3/27/2018 12:00:00 AM

US - MedicineNet

28-3-2018

FDA Panel Backs Approval of Lofexidine for Opioid Withdrawal

FDA Panel Backs Approval of Lofexidine for Opioid Withdrawal

A US Food and Drug Administration (FDA) advisory committee has recommended approval of lofexidine hydrochloride, a nonopioid, for the mitigation of symptoms in the setting of abrupt opioid withdrawal.

US - RxList

28-3-2018

FIRST AID ONLY ASPIRIN (Aspirin) Tablet, Film Coated [Acme United Corporation]

FIRST AID ONLY ASPIRIN (Aspirin) Tablet, Film Coated [Acme United Corporation]

Updated Date: Mar 28, 2018 EST

US - DailyMed

27-3-2018

Embolization Procedure Reduces Osteoarthritis Knee Pain

Embolization Procedure Reduces Osteoarthritis Knee Pain

A minimally invasive, image-guided procedure that blocks small vessels in the knee with the help of biodegradable microspheres relieves symptoms of knee osteoarthritis (OA), a small study found. In the first US clinical trial of geniculate artery embolization (GAE), the procedure provided durable results out to 6 months in 6 of 13 patients tested.

US - RxList

26-3-2018

FIRST AID ONLY IBUPROFEN (Ibuprofen) Tablet, Coated [Acme United Corporation]

FIRST AID ONLY IBUPROFEN (Ibuprofen) Tablet, Coated [Acme United Corporation]

Updated Date: Mar 26, 2018 EST

US - DailyMed

22-3-2018

School Nurses at Ground Zero for Food Allergies

School Nurses at Ground Zero for Food Allergies

Title: School Nurses at Ground Zero for Food AllergiesCategory: Health NewsCreated: 3/20/2018 12:00:00 AMLast Editorial Review: 3/21/2018 12:00:00 AM

US - MedicineNet

22-3-2018

Just How Safe Is Your Pet's Food?

Just How Safe Is Your Pet's Food?

Title: Just How Safe Is Your Pet's Food?Category: Health NewsCreated: 3/21/2018 12:00:00 AMLast Editorial Review: 3/21/2018 12:00:00 AM

US - MedicineNet