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Novartis Consumer Health Recalls
60 recalls on record · March 27, 2013 to March 5, 2014 · Drugs, Food & Beverage
Recalls by year
13
14
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 9, 2013Food & BeverageFDA
Novartis Consumer Health recalls Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings)
Hazard: The products are being recalled due to the receipt of a relatively high number of consumer complaints.
September 25, 2013Food & BeverageFDA
Novartis Consumer Health recalls Benefibre, Orange Creme Chewables, 36ct and 100ct chewable tablet bottles. Foreign labeling: Novartis Consumer Health C
Hazard: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
September 25, 2013Food & BeverageFDA
Novartis Consumer Health recalls Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippa
Hazard: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
September 25, 2013Food & BeverageFDA
Novartis Consumer Health recalls Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Hazard: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
September 25, 2013Food & BeverageFDA
Novartis Consumer Health recalls Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet bottles. Novartis Consum
Hazard: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
September 25, 2013Food & BeverageFDA
Novartis Consumer Health recalls Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis Consu
Hazard: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Nighttime Antacid with Acid Reflux Barrier (calcium carbonate and alginic acid) chewable tablets, 500 mg/200 mg,
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Nighttime Antacid with Acid Reflux Barrier (calcium carbonate and alginic acid) chewable tablets, 500 mg/200 mg,
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and simethicone) chewable tablets, 600 mg/60 mg, Wild Ber
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox, Regular Strength Antacid (calcium carbonate) chewable tablets, 600 mg, Wintergreen flavor, 50-count tablets per
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Extra Strength Antacid (calcium carbonate) chewable tablets,1000 mg, Wild Berry flavor, packaged in a) 35-count (
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and simethicone) chewable tablets, 1000 mg/60 mg,
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and simethicone) chewable tablets, 1000 mg/60 mg,
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Regular Strength Antacid (calcium carbonate) chewable tablets, 600 mg, Wild Berry flavor, packaged in a) 50-count
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 28, 2013DrugsFDA
Novartis Consumer Health recalls Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and simethicone) chewable tablets, 1000 mg/60 mg, Assorte
Hazard: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
August 14, 2013DrugsFDA
Novartis Consumer Health recalls Parsel Plus (reference US product: Excedrin Tension Headache) (Acetaminophen 500 mg and Caffeine 65 mg), packaged in 2-
Hazard: Defective container: products are packaged in pouches which may not have been fully sealed
August 14, 2013DrugsFDA
Novartis Consumer Health recalls No Doz, Max Strength (200 mg caffeine) caplets, 2-count caplets per pouch, Distributed by Novartis Consumer Health, Inc.
Hazard: Defective container: products are packaged in pouches which may not have been fully sealed
August 14, 2013DrugsFDA
Novartis Consumer Health recalls Excedrin Migraine (Acetaminophen 250 mg, Aspirin (NSAID) 250 mg and Caffeine 65 mg), a) 2-count tablets packaged in pouc
Hazard: Defective container: products are packaged in pouches which may not have been fully sealed
August 14, 2013DrugsFDA
Novartis Consumer Health recalls Excedrin Extra Strength (Acetaminophen 250 mg, Aspirin (NSAID) 250 mg and Caffeine 65 mg), a) 2-ct tablets in pouches b
Hazard: Defective container: products are packaged in pouches which may not have been fully sealed
June 12, 2013DrugsFDA
Novartis Consumer Health recalls Voltaren Gel (diclofenac sodium topical gel) 1%, for topical use only, RX only, a) Packaged in 20 gm tubes, NDC 63481-68
Hazard: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
June 12, 2013DrugsFDA
Novartis Consumer Health recalls Lamisil AT Cream (terbinafine hydrochloride 1% antifungal), 12 gm ( .42 oz) Tubes and 30 gm (1 oz) Tubes packaged in one
Hazard: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
June 12, 2013DrugsFDA
Novartis Consumer Health recalls Novartis Lamisil AT Cream for Jock Itch (terbinafine hydrochloride 1% antifungal), a) 12 g (.42 oz) Tube, NDC 0067-3999
Hazard: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
June 12, 2013DrugsFDA
Novartis Consumer Health recalls Target Up & Up, athlete's foot cream, full prescription strength, terbinafine hydrochloride 1% antifungal, 30 g (1 oz),
Hazard: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot..
June 12, 2013DrugsFDA
Novartis Consumer Health recalls Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany, N
Hazard: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
May 29, 2013DrugsFDA
Novartis Consumer Health recalls Lamisil AT (terbinafine hydrochloride cream 1% antifungal), 24 g (.85 oz) tube, Novartis Consumer Health, Parsippany, NJ
Hazard: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
March 27, 2013DrugsFDA
Novartis Consumer Health recalls 4 way Saline Moisturizing Mist with Eucalyptol & Menthol, 1-fl. oz. bottles, OTC. Distributed by Novartis Consumer Healt
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.
March 27, 2013DrugsFDA
Novartis Consumer Health recalls 4 way Nasal Decongestant Menthol Nasal Spray, containing phenylephrine hydrochloride 1%, a) 1/2-fl. oz. bottles (NDC 006
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.
March 27, 2013DrugsFDA
Novartis Consumer Health recalls 4 way Nasal Decongestant Fast Acting Nasal Spray, containing phenylephrine hydrochloride 1%, a) 1/2-fl. oz. bottles (NDC
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.
March 27, 2013DrugsFDA
Novartis Consumer Health recalls Nupercainal, Dibucaine, Hemorrhoidal & Topical Analgesic Ointment, a) 1-oz. tubes (NDC 0067-5812-96), b) 2-oz. tubes (ND
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.
March 27, 2013DrugsFDA
Novartis Consumer Health recalls Myoflex (trolamine salicylate) 10%, Pain Relieving Cream, a) 2-oz tube, b) 4-oz. tube, OTC. The firm name on the label i
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.