Label: PEPCID COMPLETE- famotidine, calcium carbonate, and magnesium hydroxide tablet, chewable
- NDC Code(s): 16837-891-25, 16837-891-50, 16837-891-65, 16837-891-66
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated October 25, 2024
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Use
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Warnings
Do not use
- if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
- with other acid reducers
Ask a doctor before use if you have
- had heartburn over 3 months. This may be a sign of a more serious condition.
- heartburn with lightheadedness, sweating, or dizziness
- chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
- frequent chest pain
- frequent wheezing, particularly with heartburn
- unexplained weight loss
- nausea or vomiting
- stomach pain
- kidney disease
Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids and acid reducers may interact with certain prescription drugs.
- Directions
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INGREDIENTS AND APPEARANCE
PEPCID COMPLETE
famotidine, calcium carbonate, and magnesium hydroxide tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:16837-891 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE 10 mg CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 800 mg MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 165 mg Inactive Ingredients Ingredient Name Strength CELLULOSE ACETATE (UNII: 3J2P07GVB6) STARCH, CORN (UNII: O8232NY3SJ) CROSPOVIDONE (UNII: 2S7830E561) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM) ACACIA (UNII: 5C5403N26O) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MINERAL OIL (UNII: T5L8T28FGP) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color green Score no score Shape ROUND Size 18mm Flavor MINT Imprint Code P Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:16837-891-25 25 in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2009 2 NDC:16837-891-50 50 in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2009 3 NDC:16837-891-65 25 in 1 BOTTLE; Type 0: Not a Combination Product 01/11/2024 4 NDC:16837-891-66 50 in 1 BOTTLE; Type 0: Not a Combination Product 12/14/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020958 03/01/2009 Labeler - Johnson & Johnson Consumer Inc. (878046358)