Over the Counter Medications with Generic Names Beginning ‘F’, Page 15

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Acid Reducer (Famotidine)

Relieves heartburn associated with acid indigestion and sour stomach, prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food…

Publix Super Markets Inc25 November 2019

Acid Reducer Original Strength (Famotidine)

Relieves heartburn associated with acid indigestion and sour stomach, prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food…

Rite Aid Corporation2 December 2019

Acid Reducer Maximum Strength (Famotidine)

Relieves heartburn associated with acid indigestion and sour stomach, prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food…

Meijer Distribution Inc5 December 2019

Acid Controller (Famotidine)

Relieves heartburn associated with acid indigestion and sour stomach, prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food…

Shopko Stores Operating Co., LLC9 December 2019

Famotidine

Relieves heartburn associated with acid indigestion and sour stomach, prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food…

Wal-Mart Stores Inc10 December 2019

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FDA Medwatch

Fusion Health and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and Immune Boost Sublingual Vitamin D3 Due to the Unapproved Use of a Food Additive and Unapproved Marketing Statements
Sun, 22 Nov 2020. Fusion Health and Vitality LLC is voluntarily recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune…
Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine
Wed, 18 Nov 2020. Fresenius Kabi USA is voluntarily recalling a single lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present…

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As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.