FIRST FOOD
Main information
- Trade name:
- FIRST FOOD 400G
- Available from:
- Wockhardt
- Composition:
- 400G
- Medicine domain:
- Humans
- Medicine type:
- Allopathic drug
Documents
- for the general public:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- for healthcare professionals:
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for healthcare professionals.
Localization
- Available in:
-
India
- Language:
- English
Other information
Status
- Source:
- Central Drugs Standard Control Organization
- Last update:
- 09-08-2016
- The information leaflet for this product is not currently available, you can send a request to our customer service and we will notify you as soon as we are able to obtain it.
Request the information leaflet for the general public.
- Access to this document is only available to registered users.
Register now for full access
18-4-2018
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 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 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
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 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 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
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
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, 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 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
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 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 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
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>
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
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
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
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
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
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
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 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
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 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
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
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. 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 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
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
First medicine to be granted a provisional approval determination
Therapeutic Goods Administration - Australia
14-4-2018
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
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
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 #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 #MedicalDevice
FDA - U.S. Food and Drug Administration
11-4-2018
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
FDA OKs First Transitional Contacts That Darken in Sunlight
US - eMedicineHealth
10-4-2018
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
9-4-2018
GREEN GUARD MAXIMUM STRENGTH STOMACH RELIEF (Calcium Carbonate 750 Mg) Tablet, Chewable [Unifirst First Aid Corporation]
Updated Date: Apr 9, 2018 EST
US - DailyMed
9-4-2018
HANDY SOLUTIONS FIRST AID KIT ANTISEPTIC TOWELETTE (Benzalkonium Chloride) Kit [Navajo Manufacturing Company Inc.]
Updated Date: Apr 9, 2018 EST
US - DailyMed
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
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
6-4-2018
UEC MEDICAL FIRST AID ANTIBIOTIC (Bacitracin Zinc) Ointment [United Exchange Corp.]
Updated Date: Apr 6, 2018 EST
US - DailyMed
6-4-2018
UEC MEDICAL FIRST AID ANTIBIOTIC (Bacitracin Zinc, Neomycin Sulfate, And Polymyxin B Sulfate) Ointment [United Exchange Corp.]
Updated Date: Apr 6, 2018 EST
US - DailyMed
5-4-2018
TARTAR CONTROL PLUS (Eucalyptol, Menthol, Methyl Salicylate, Thymol) Mouthwash [Wegmans Food Markets]
Updated Date: Apr 5, 2018 EST
US - DailyMed
4-4-2018
FIRST AID BACITRAYCIN PLUS ORIGINAL (Bacitracin) Ointment [First Aid Research Corp.]
Updated Date: Apr 4, 2018 EST
US - DailyMed
3-4-2018
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
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
3-4-2018
MEDIQUE ASPIRIN (Aspirin) Tablet, Film Coated MEDI-FIRST ASPIRIN (Aspirin) Tablet, Film Coated MEDI FIRST PLUS ASPIRIN (Aspirin) Tablet, Film Coated [Unifirst First Aid Corporation]
Updated Date: Apr 3, 2018 EST
US - DailyMed
2-4-2018
MEDIQUE APAP (Acetaminophen) Tablet, Film Coated MEDI-FIRST NON-ASPIRIN (Acetaminophen) Tablet, Film Coated MEDI FIRST PLUS NON-ASPIRIN (Acetaminophen) Tablet, Film Coated DOVER AMINOPHEN (Acetaminophen) Tablet, Film Coated [Unifirst First Aid Corporation
Updated Date: Apr 2, 2018 EST
US - DailyMed
2-4-2018
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.]
Updated Date: Apr 2, 2018 EST
US - DailyMed
2-4-2018
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
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 #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]
Updated Date: Mar 29, 2018 EST
US - DailyMed
29-3-2018
FIRST AID ONLY EXTRA-STRENGTH NON-ASPIRIN (Acetaminophen) Tablet, Film Coated [Acme United Corporation]
Updated Date: Mar 29, 2018 EST
US - DailyMed
28-3-2018
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
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
MEDIQUE APAP EXTRA STRENGTH (Acetaminophen) Tablet, Film Coated MEDI-FIRST NON-ASPIRIN EXTRA STRENGTH (Acetaminophen) Tablet, Film Coated MEDI FIRST PLUS NON-ASPIRIN EXTRA STRENGTH (Acetaminophen) Tablet, Film Coated [Unifirst First Aid Corporation]
Updated Date: Mar 28, 2018 EST
US - DailyMed
28-3-2018
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
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]
Updated Date: Mar 26, 2018 EST
US - DailyMed
22-3-2018
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?
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
