Label: EQUATE ACID REDUCER COMPLETE- famotidine, calcium carbonate, magnesium hydroxide tablet, chewable
- NDC Code(s): 49035-546-63, 49035-546-71, 49035-546-98
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 12, 2024
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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SEE NEW WARNINGS
Compare to Pepcid Complete® active ingredients
DUAL ACTION
Acid Reducer Complete
Famotidine 10 mg, Calcium Carbonate 800 mg, Magnesium Hydroxide 165 mg Tablets (Chewable)
Actual Size
Acid Reducer Plus Antacid
Just one tablet relieves heartburn due to acid indigestion
Cool Mint Flavor
50 CHEWABLE TABLETS
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INGREDIENTS AND APPEARANCE
EQUATE ACID REDUCER COMPLETE
famotidine, calcium carbonate, magnesium hydroxide tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-546 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 ASPARTAME (UNII: Z0H242BBR1) DEXTRATES (UNII: G263MI44RU) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) FERRIC OXIDE RED (UNII: 1K09F3G675) 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:49035-546-63 25 in 1 BOTTLE; Type 0: Not a Combination Product 08/08/2008 07/12/2016 2 NDC:49035-546-71 50 in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2011 3 NDC:49035-546-98 75 in 1 BOTTLE; Type 0: Not a Combination Product 10/22/2013 05/27/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077355 08/08/2008 Labeler - Wal-Mart Stores Inc (051957769)