Active Ingredient (In Each Tablet)
Famotidine, USP 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Heb for the product Famotidine (NDC 37808-036). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, warnings, do not use, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Famotidine, USP 20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
Ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, pregelatinized starch, talc, titanium dioxide
Call 1-800-406-7984
Tips for Managing Heartburn
Compare to Maximum Strength Pepcid AC®active ingredient†
NDC 37808-036-26
H-E-B®
ACID CONTROLLER
Famotidine Tablets, USP 20 mg
Acid Reducer
Maximum Strength
25 Tablets
Distributed by: H-E-B
5108231/1402
* Please review the disclaimer below.