Label: ACID REDUCER COMPLETE- famotidine, calcium carbonate, magnesium hydroxide tablet, chewable
- NDC Code(s): 21130-786-63, 21130-786-71
- Packager: Safeway
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated October 14, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients (in each chewable tablet)
- Purposes
- Use
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Warnings
Allergy alert: Do not use if you are allergic to famotidine or other acid reducers
Do not use
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- 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
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- had heartburn over 3 months. This may be a sign of a more serious condition.
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- heartburn with lightheadedness, sweating, or dizziness
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- chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
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- frequent chest pain
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- frequent wheezing, particularly with heartburn
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- unexplained weight loss
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- nausea or vomiting
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- stomach pain
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- 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
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
COMPARE TO Pepcid Complete® active ingredients
Signature SELECTTM
SEE NEW WARNINGS
DUAL ACTION
ACID REDUCER COMPLETE
Actual Size
FAMOTIDINE 10mg, CALCIUM CARBONATE 800 mg, MAGNESIUM HYDROXIDE 165 mg TABLETS (CHEWABLE)
ACID REDUCER + ANTACID
COOL MINT FLAVOR
25 CHEWABLE TABLETS
Just One Tablet! Relieves Heartburn Due to Acid Indigestion
-
INGREDIENTS AND APPEARANCE
ACID REDUCER COMPLETE
famotidine, calcium carbonate, magnesium hydroxide tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-786 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 CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 800 mg MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 165 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) ASPARTAME (UNII: Z0H242BBR1) DEXTRATES (UNII: G263MI44RU) FERRIC OXIDE RED (UNII: 1K09F3G675) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color ORANGE (PEACH WITH WHITE SPECKLES) Score no score Shape ROUND Size 18mm Flavor MINT Imprint Code L546 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-786-63 25 in 1 BOTTLE; Type 0: Not a Combination Product 09/29/2025 2 NDC:21130-786-71 50 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077355 09/22/2025 Labeler - Safeway (009137209)

