ENERZAL 200 ORANGE

Main information

  • Trade name:
  • ENERZAL 200 ORANGE 200ML
  • Composition:
  • 200ML
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • ENERZAL 200 ORANGE 200ML
    India
  • Language:
  • English

Other information

Status

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

20-3-2018

Vietti Foods Issues Allergy Alert on Undeclared Wheat and Eggs in Southgate Hot Dog Chili Sauce

Vietti Foods Issues Allergy Alert on Undeclared Wheat and Eggs in Southgate Hot Dog Chili Sauce

Vietti Foods is recalling approximately 200 cases of 15 oz cans of Southgate Hot Dog Chili Sauce, UPC 0 71846 95242 6, LOT # P642 M1217 70026. This recall has been initiated due to mislabeling because some of the cans may contain Dumplings with Chicken instead of Hot Dog Chili Sauce.

FDA - U.S. Food and Drug Administration

16-3-2018

Orange Book Zip File

Orange Book Zip File

Orange Book Data Files (compressed)

FDA - U.S. Food and Drug Administration

16-3-2018

Bayer Issues Voluntary Recall of Alka-Seltzer Plus® Products

Bayer Issues Voluntary Recall of Alka-Seltzer Plus® Products

Bayer is voluntarily recalling Alka-Seltzer Plus® packages that: • Were sold only in the U.S. at Walmart, CVS, Walgreens and Kroger (including Dillons Food Stores, Fred Meyer, Fry’s Food Stores, Ralphs, King Soopers and Smith’s Food and Drug) after February 9, 2018. • Can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or green background, the product is included in the recall (please see attached photos). The affected...

FDA - U.S. Food and Drug Administration

1-3-2018

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company is recalling approximately 200 cases of its Cherry SKI product because they are incorrectly labeled. Only the Cherry SKI products with the new design are being recalled, which were delivered to the southern Illinois, Evansville, IN and Winchester, OH markets.

FDA - U.S. Food and Drug Administration

13-1-2018

Hiland Dairy Announces Voluntary Recall Of Hiland Dairy Orange Juice And Tampico Citrus Punch

Hiland Dairy Announces Voluntary Recall Of Hiland Dairy Orange Juice And Tampico Citrus Punch

Hiland Dairy is announcing a voluntary recall of two products produced at the Omaha, Nebraska facility, over concerns the products may contain milk protein that could affect those individuals that have sensitivity to milk allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. No illnesses or allergic reactions have been reported at this time.

FDA - U.S. Food and Drug Administration

12-1-2018

Fieldbrook Foods Corporation Clarifies Scope of its Voluntary Recall. Products Include Orange Cream

Fieldbrook Foods Corporation Clarifies Scope of its Voluntary Recall. Products Include Orange Cream

Fieldbrook Foods Corporation is clarifying that the previously announced voluntary recall of all orange cream bars and chocolate coated vanilla ice cream bars that were produced in 2017 on the company’s Hoyer 1 Line at its Dunkirk, NY plant (plant code 362677) also includes 28,751 cases of Raspberry Cream Bars that were included with Orange Cream Bars in ALDI seasonal split-case purchases.

FDA - U.S. Food and Drug Administration

10-1-2018

Fieldbrook Foods Corporation, Announces an Extension of Voluntary Recall of Orange Cream Bars and Chocolate Coated Vanilla Ice Cream Bars for Possible Health Risk

Fieldbrook Foods Corporation, Announces an Extension of Voluntary Recall of Orange Cream Bars and Chocolate Coated Vanilla Ice Cream Bars for Possible Health Risk

Fieldbrook Foods Corporation has issued a voluntary recall of all orange cream bars and chocolate coated vanilla ice cream bars that were produced in 2017 on the company’s Hoyer 1 Line at its Dunkirk, NY plant (plant code 362677). This is the only production line and the only Fieldbrook Foods plant (of 3) involved in this recall notice. Both products are being recalled due to the possibility that they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal...

FDA - U.S. Food and Drug Administration

6-1-2018

Fieldbrook Foods Corporation, Announces a Voluntary Recall of Orange Cream Bars for Possible Health Risk

Fieldbrook Foods Corporation, Announces a Voluntary Recall of Orange Cream Bars for Possible Health Risk

Fieldbrook Foods Corporation of Dunkirk NY has issued a voluntary recall of 20 cases of the Tops brand of Orange Cream Bars and 320 cases of the Meijer Purple Cow brand Orange Cream Bars due to the possibility that the product may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fev...

FDA - U.S. Food and Drug Administration

14-12-2017

Marmex Corp Issues Voluntary Nationwide Recall Of Blue Pearl All Natural Male Enhancement Supplement, Due To Undeclared Sildenafil

Marmex Corp Issues Voluntary Nationwide Recall Of Blue Pearl All Natural Male Enhancement Supplement, Due To Undeclared Sildenafil

Orange, CA, Marmex Corp is voluntarily recalling All lots of Blue Pearl All Natural Male Enhancement Supplement, 500mg to the consumer level. FDA analysis has found the products to contain sildenafil.

FDA - U.S. Food and Drug Administration

5-10-2017

Surflink Media and Surflink Media 2 (Models 200 and 210) - used with wireless hearing aids

Surflink Media and Surflink Media 2 (Models 200 and 210) - used with wireless hearing aids

Recall for product correction - may cause interference with mobile towers

Therapeutic Goods Administration - Australia

20-9-2017

Nature Supplement Inc. Issues Voluntary Florida Recall of Vegetable Vigra Due to Undeclared Sildenafil

Nature Supplement Inc. Issues Voluntary Florida Recall of Vegetable Vigra Due to Undeclared Sildenafil

Natures Supplement, Inc. is voluntarily recalling 260 bottles of VEGETABLE VIGRA, 200 mg capsules to the consumer level. FDA analysis found this product to be tainted with Sidenafil. Sildenafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of Sildenafil in the Vegetable Vigra product renders it an unapproved drug for which safety and efficacy has not been established, therefore subject to recall.

FDA - U.S. Food and Drug Administration

22-8-2017



Chargenrückruf - Voriconazol Sandoz® 200mg, Filmtabletten

Chargenrückruf - Voriconazol Sandoz® 200mg, Filmtabletten

Swissmedic - Swiss Agency for Therapeutic Products

18-4-2018

ORANGE VANILLA SPF30 (Zinc Oxide) Stick [Crossing Cultures LLC Dba Goddess Garden]

ORANGE VANILLA SPF30 (Zinc Oxide) Stick [Crossing Cultures LLC Dba Goddess Garden]

Updated Date: Apr 18, 2018 EST

US - DailyMed

17-4-2018

Company Recalls More Than 200 Million Eggs Due to Salmonella Scare

Company Recalls More Than 200 Million Eggs Due to Salmonella Scare

Title: Company Recalls More Than 200 Million Eggs Due to Salmonella ScareCategory: Health NewsCreated: 4/15/2018 12:00:00 AMLast Editorial Review: 4/16/2018 12:00:00 AM

US - MedicineNet

13-4-2018

A-6 (Lemon, Orange, And Grapefruit) Solution [DNA Labs, Inc.]

A-6 (Lemon, Orange, And Grapefruit) Solution [DNA Labs, Inc.]

Updated Date: Apr 13, 2018 EST

US - DailyMed

5-4-2018

CLEANWELL NATURAL ORANGE VANILLA HAND SANITIZER Spray [CleanWell, LLC]

CLEANWELL NATURAL ORANGE VANILLA HAND SANITIZER Spray [CleanWell, LLC]

Updated Date: Apr 5, 2018 EST

US - DailyMed

4-4-2018

CLEANWELL NATURAL ORANGE VANILLA HAND SANITIZING WIPES Cloth [CleanWell, LLC]

CLEANWELL NATURAL ORANGE VANILLA HAND SANITIZING WIPES Cloth [CleanWell, LLC]

Updated Date: Apr 4, 2018 EST

US - DailyMed

26-3-2018

HAND SANITIZER ORANGE BLOSSOM (Organic Ethyl Alcohol) Gel [Whole Foods Market, Inc.]

HAND SANITIZER ORANGE BLOSSOM (Organic Ethyl Alcohol) Gel [Whole Foods Market, Inc.]

Updated Date: Mar 26, 2018 EST

US - DailyMed

26-2-2018

EU/3/18/1984 (Omeros London Limited)

EU/3/18/1984 (Omeros London Limited)

EU/3/18/1984 (Active substance: Recombinant human monoclonal antibody against mannan-binding lectin-associated serine protease-2) - Orphan designation - Commission Decision (2018)1251 of Mon, 26 Feb 2018 European Medicines Agency (EMA) procedure number: EMA/OD/200/17

Europe -DG Health and Food Safety

21-2-2018

HAND SANITIZER ORANGE (Alcohol) Gel [JFL ENTERPRISES, INC]

HAND SANITIZER ORANGE (Alcohol) Gel [JFL ENTERPRISES, INC]

Updated Date: Feb 21, 2018 EST

US - DailyMed

21-2-2018

ENDURE 200 (Triclosan) Solution [Ecolab Inc.]

ENDURE 200 (Triclosan) Solution [Ecolab Inc.]

Updated Date: Feb 21, 2018 EST

US - DailyMed

2-1-2018

NATURES ANTIBAC ORANGE VANILLA Soap [CleanWell, LLC]

NATURES ANTIBAC ORANGE VANILLA Soap [CleanWell, LLC]

Updated Date: Jan 2, 2018 EST

US - DailyMed

2-1-2018

CLEANWELL NATURAL ANTIBACTERIAL FOAMING ORANGE VANILLA Soap [CleanWell, LLC]

CLEANWELL NATURAL ANTIBACTERIAL FOAMING ORANGE VANILLA Soap [CleanWell, LLC]

Updated Date: Jan 2, 2018 EST

US - DailyMed

29-12-2017

ANTI-BACTERIAL HAND ORANGE GINGER (Alcohol) Gel [Bath Body Works, Inc.]

ANTI-BACTERIAL HAND ORANGE GINGER (Alcohol) Gel [Bath Body Works, Inc.]

Updated Date: Dec 29, 2017 EST

US - DailyMed

19-12-2017

REVALOR-200 (Trenbolone Acetate And Estradiol) Implant [Merck Sharp Dohme Corp.]

REVALOR-200 (Trenbolone Acetate And Estradiol) Implant [Merck Sharp Dohme Corp.]

Updated Date: Dec 19, 2017 EST

US - DailyMed

14-12-2017

ANTI-AGING FOUNDATION SPF 15 SHADE 200 (Octinoxate) Emulsion [La Prairie, Inc.]

ANTI-AGING FOUNDATION SPF 15 SHADE 200 (Octinoxate) Emulsion [La Prairie, Inc.]

Updated Date: Dec 14, 2017 EST

US - DailyMed

8-12-2017

DRAMAMINE ORANGE (Dimenhydrinate) Tablet, Chewable [Medtech Products Inc.]

DRAMAMINE ORANGE (Dimenhydrinate) Tablet, Chewable [Medtech Products Inc.]

Updated Date: Dec 8, 2017 EST

US - DailyMed

22-11-2017

PCXX VANILLA ORANGE NEUTRAL F (Sodium Fluoride) Aerosol, Foam [Ross Healthcare Inc.]

PCXX VANILLA ORANGE NEUTRAL F (Sodium Fluoride) Aerosol, Foam [Ross Healthcare Inc.]

Updated Date: Nov 22, 2017 EST

US - DailyMed

21-11-2017

MOOREBRAND IBUPROFEN (I Buprofen 200 Mg) Tablet, Film Coated [Moore Medical LLC]

MOOREBRAND IBUPROFEN (I Buprofen 200 Mg) Tablet, Film Coated [Moore Medical LLC]

Updated Date: Nov 21, 2017 EST

US - DailyMed

20-11-2017

IBUPROFEN 200MG Tablet, Coated [Athlete'S Needs, Inc.]

IBUPROFEN 200MG Tablet, Coated [Athlete'S Needs, Inc.]

Updated Date: Nov 20, 2017 EST

US - DailyMed

16-11-2017

SOUND BODY IBUPROFEN (Ibuprofen 200 Mg) Capsule, Liquid Filled [Allegiant Health]

SOUND BODY IBUPROFEN (Ibuprofen 200 Mg) Capsule, Liquid Filled [Allegiant Health]

Updated Date: Nov 16, 2017 EST

US - DailyMed

30-10-2017

MUCUS RELIEF (Guaifenesin 200 Mg) Tablet [Richmond Pharmaceuticals, Inc.]

MUCUS RELIEF (Guaifenesin 200 Mg) Tablet [Richmond Pharmaceuticals, Inc.]

Updated Date: Oct 30, 2017 EST

US - DailyMed

28-8-2017

ISLEAF SHINE SMOOTH LIP GLAZE ORANGE (Mineral Oil) Liquid [C3 Co., Ltd.]

ISLEAF SHINE SMOOTH LIP GLAZE ORANGE (Mineral Oil) Liquid [C3 Co., Ltd.]

Updated Date: Aug 28, 2017 EST

US - DailyMed

8-8-2017

ISLEAF SATIN LIP AND CHEEK DUO CORAL ORANGE (Dimethicone) Liquid [C3 Co., Ltd.]

ISLEAF SATIN LIP AND CHEEK DUO CORAL ORANGE (Dimethicone) Liquid [C3 Co., Ltd.]

Updated Date: Aug 8, 2017 EST

US - DailyMed