Gluten Screen

Last verified May 17, 2026 · 10 product labels screened

Is famotidine gluten-free?

Looks mostly clean — worth verifying with the maker. Mostly yes — but worth a quick call to the manufacturer for some generics. Of 10 product labels we checked, 8 are clean, 0 are confirmed gluten-free by the maker, and 2 contain an inactive ingredient (typically a source-ambiguous starch) whose botanical origin isn't fully disclosed. None contained confirmed gluten.

Drug context

About famotidine

Famotidine is an H2 blocker used for heartburn and ulcers, sold under brand names including Pepcid.

Why this matters

Different manufacturers, different ingredients

Generics of famotidine use the same active ingredient, but they aren't required to use the same inactive ingredients. Your pharmacy may switch which manufacturer they dispense between fills, sometimes without telling you. The list below shows each manufacturer's product label as a separate entry, because that's the granularity that actually matters when you're celiac.

The labels

The 10 we checked

  1. 01
    ST. MARY'S MEDICAL PARK PHARMACY worth a call to confirm

    US label (DailyMed) · FAMOTIDINE TABLET, FILM COATED [ST. MARY'S MEDICAL PARK PHARMACY] · label dated May 04, 2026

    Worth a call to the maker: SODIUM STARCH GLYCOLATE TYPE A

    Inactive ingredients HYDROXYPROPYL CELLULOSE, UNSPECIFIED · HYPROMELLOSE, UNSPECIFIED · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · SODIUM STARCH GLYCOLATE TYPE A · STARCH, CORN · TITANIUM DIOXIDE · TRIACETIN

    View source label →
  2. 02
    CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED worth a call to confirm

    US label (DailyMed) · COMPLETE ACID REDUCER (FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE) TABLET, CHEW… · label dated Apr 14, 2026

    Worth a call to the maker: SODIUM STARCH GLYCOLATE TYPE A

    Inactive ingredients ANHYDROUS LACTOSE · D&C YELLOW NO. 10 ALUMINUM LAKE · DEXTRATES · FD&C YELLOW NO. 6 ALUMINUM LAKE · GLYCERYL MONOSTEARATE · LACTOSE MONOHYDRATE · MAGNESIUM STEARATE · MALTODEXTRIN · MICROCRYSTALLINE CELLULOSE · POLYSORBATE 80 · POVIDONE, UNSPECIFIED · SODIUM STARCH GLYCOLATE TYPE A · SUCRALOSE · TALC

    View source label →
  3. 03
    L. Perrigo Company nothing flagged on the label

    US label (DailyMed) · GOOD SENSE ACID REDUCER (FAMOTIDINE) TABLET, FILM COATED [L. PERRIGO COMPANY] · label dated May 13, 2026

    Inactive ingredients CARNAUBA WAX · CROSCARMELLOSE SODIUM · LACTOSE MONOHYDRATE · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYVINYL ALCOHOL, UNSPECIFIED · SILICON DIOXIDE · TALC · TITANIUM DIOXIDE

    View source label →
  4. 04
    HyVee Inc nothing flagged on the label

    US label (DailyMed) · ACID REDUCER ORIGINAL STRENGTH (FAMOTIDINE) TABLET, FILM COATED [HYVEE INC] · label dated May 13, 2026

    Inactive ingredients CARNAUBA WAX · FERRIC OXIDE RED · FERRIC OXIDE YELLOW · HYPROMELLOSE, UNSPECIFIED · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYDEXTROSE · POLYETHYLENE GLYCOL, UNSPECIFIED · TALC · TITANIUM DIOXIDE · TRIACETIN

    View source label →
  5. 05
    Walgreen Company nothing flagged on the label

    US label (DailyMed) · ACID CONTROLLER (FAMOTIDINE) TABLET, FILM COATED [WALGREEN COMPANY] · label dated Apr 29, 2026

    Inactive ingredients CARNAUBA WAX · CROSCARMELLOSE SODIUM · LACTOSE MONOHYDRATE · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYVINYL ALCOHOL, UNSPECIFIED · SILICON DIOXIDE · TALC · TITANIUM DIOXIDE

    View source label →
  6. 06
    Par Health USA, LLC nothing flagged on the label

    US label (DailyMed) · IBUPROFEN AND FAMOTIDINE TABLET [PAR HEALTH USA, LLC] · label dated Apr 23, 2026

    Inactive ingredients ANHYDROUS LACTOSE · CROSCARMELLOSE SODIUM · FD&C BLUE NO. 1 ALUMINUM LAKE · FD&C BLUE NO. 2--ALUMINUM LAKE · HYPROMELLOSE, UNSPECIFIED · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYSORBATE 80 · POLYVINYL ALCOHOL, UNSPECIFIED · POVIDONE K30 · SILICON DIOXIDE · TALC · TITANIUM DIOXIDE

    View source label →
  7. 07
    CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED nothing flagged on the label

    US label (DailyMed) · ACID REDUCER (FAMOTIDINE) TABLET, FILM COATED [CVS WOONSOCKET PRESCRIPTION CENTER, INCO… · label dated Apr 14, 2026

    Inactive ingredients CARNAUBA WAX · CROSCARMELLOSE SODIUM · LACTOSE MONOHYDRATE · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYVINYL ALCOHOL, UNSPECIFIED · SILICON DIOXIDE · TALC · TITANIUM DIOXIDE

    View source label →
  8. 08
    CVS Pharmacy nothing flagged on the label

    US label (DailyMed) · ACID CONTROLLER (FAMOTIDINE) TABLET, FILM COATED [CVS PHARMACY] · label dated Apr 13, 2026

    Inactive ingredients CARNAUBA WAX · CROSCARMELLOSE SODIUM · LACTOSE MONOHYDRATE · MAGNESIUM STEARATE · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYVINYL ALCOHOL, UNSPECIFIED · SILICON DIOXIDE · TALC · TITANIUM DIOXIDE

    View source label →
  9. 09
    PHOENIX RX LLC nothing flagged on the label

    US label (DailyMed) · IBUPROFEN AND FAMOTIDINE TABLET, FILM COATED [PHOENIX RX LLC] · label dated Apr 09, 2026

    Inactive ingredients AMMONIA · CROSCARMELLOSE SODIUM · FD&C BLUE NO. 1 · FD&C BLUE NO. 2 · FERROSOFERRIC OXIDE · HYPROMELLOSE, UNSPECIFIED · MICROCRYSTALLINE CELLULOSE · POLYETHYLENE GLYCOL, UNSPECIFIED · POLYVINYL ALCOHOL, UNSPECIFIED · PROPYLENE GLYCOL · SHELLAC · SILICON DIOXIDE · TALC · TITANIUM DIOXIDE

    View source label →
  10. 10
    Medical Purchasing Solutions, LLC nothing flagged on the label

    US label (DailyMed) · FAMOTIDINE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC] · label dated Apr 06, 2026

    Inactive ingredients ASPARTIC ACID · MANNITOL · WATER

    View source label →

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Background

What “gluten in a medication” actually means

Gluten enters drugs through their excipients — the inactive ingredients used to bind, coat, fill, or stabilize the dose. The main concern is wheat starch as a filler. Source-ambiguous starches (plain “starch”, pregelatinized starch, sodium starch glycolate, modified starch) get flagged for verification because their botanical origin isn't always disclosed on the label.

The 2024 Mangione et al. pediatric NDC analysis (689 NDCs across the top 100 pediatric medications) found 1.5% contained gluten outright; another 25.7% couldn't be confirmed either way. Liquid and oral-suspension formulations carry disproportionate risk because wheat starch is a common thickener. Full methodology →

Keep checking

Other drugs people look up

Important. This page is informational. Drug labels can change without notice; a manufacturer attestation is point-in-time, not a warranty. If you have celiac disease and your pharmacy switches manufacturers, re-screen the new label before taking the dispensed product. For a definitive answer, call the manufacturer's medical-information line with the NDC code from your prescription bottle.