Label: SOUND HEALTH HEARTBURN AND GAS CHEWS- calcium carbonate tablet, chewable
- NDC Code(s): 52642-035-82
- Packager: BestCo Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 6, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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ASK DOCTOR
Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain persription drugs.
Do not take more than 5 chewable tablets in a 24-hour period, or use the maxium dosage for more than 2 weeks, except under the advice and supervision of a physician.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients: Acacia gum, beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup, FD&C blue no. 1 aluminum lake, FD&C Blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, hydrogenated coconut oil, modified corn starch, natural and artificial flavors, phosphoric acid, pregelatinized corn starch, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose and titanium dioxide.
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INGREDIENTS AND APPEARANCE
SOUND HEALTH HEARTBURN AND GAS CHEWS
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52642-035 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 750 mg DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color pink Score score with uneven pieces Shape ROUND Size 14mm Flavor BERRY Imprint Code DR Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52642-035-82 82 in 1 BOTTLE; Type 0: Not a Combination Product 12/27/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 12/27/2019 Labeler - BestCo Inc. (002149136) Registrant - BestCo Inc. (002149136) Establishment Name Address ID/FEI Business Operations Bestco Inc. 002149136 manufacture(52642-035)