NDC | 41250-284-71 |
Set ID | 6e8ed233-9ffb-46f7-9632-d5bc3d3a558b |
Category | HUMAN OTC DRUG LABEL |
Packager | Meijer Distribution Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | ANDA077355 |
- 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.
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- 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
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Inactive ingredients
anhydrous lactose, artificial berry flavor, aspartame, D&C red no. 7 calcium lake, dextrates, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, glyceryl monostearate, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyacrylate dispersion, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, talc
- Questions or comments?
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Principal Display Panel
Compare to Pepcid Complete® active ingredients
dual action complete
Famotidine 10 mg | Calcium Carbonate 800 mg
Magnesium Hydroxide 165 mg Tablets (Chewable)
Acid Reducer + Antacid
SEE NEW WARNINGS
HEARTBURN RELIEF | Just One Tablet!
Relieves Heartburn Due to Acid Indigestion
50 Chewable Tablets | actual size
Berry Flavor
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INGREDIENTS AND APPEARANCE
DUAL ACTION COMPLETE
famotidine, calcium carbonate and magnesium hydroxide tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-284 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FAMOTIDINE (UNII: 5QZO15J2Z8) (FAMOTIDINE - UNII:5QZO15J2Z8) FAMOTIDINE 10 mg MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE 165 mg CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 800 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) ASPARTAME (UNII: Z0H242BBR1) D&C RED NO. 7 (UNII: ECW0LZ41X8) DEXTRATES (UNII: G263MI44RU) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color PINK (mottled) Score no score Shape ROUND (bi-layered) Size 17mm Flavor BERRY Imprint Code L321 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-284-71 50 in 1 BOTTLE; Type 0: Not a Combination Product 01/26/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077355 01/26/2016 Labeler - Meijer Distribution Inc (006959555)