Label: ASSORTED FRUIT ANTACID FLAVOR CHEWS- calcium carbonate tablet, chewable
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-748-12 - Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 9, 2019
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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- OTHER SAFETY INFORMATION
- PREGNANCY OR BREAST FEEDING
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- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients: Beeswax, carmine, carnauba wax, citric acid, corn syrup, DL-alpha tocopherol, ethyl acetate, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, FD&C yellow no. 5 lake (tartrazine), FD&C yellow no. 6, FD&C yellow no. 6 aluminum lake, gum arabic, hydrogenated coconut oil, medium chain triglycerides, methyl paraben, modified corn starch, natural and artificial flavors, pregelatinized corn starch, propylene glycol, propyl paraben, phosphoric acid, purified water, shellic, sodium benzoate, sorbic acid, sorbitol, soy lecithin, soybean oil, sucrose and titanium dioxide.
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INGREDIENTS AND APPEARANCE
ASSORTED FRUIT ANTACID FLAVOR CHEWS
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-748 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 Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) Product Characteristics Color pink (Orange, Pink and Yellow) Score no score Shape ROUND Size 14mm Flavor FRUIT Imprint Code FC Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-748-12 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 06/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 06/01/2015 Labeler - CVS Pharmacy (062312574) Registrant - Bestco Inc (002149136) Establishment Name Address ID/FEI Business Operations Bestco Inc 002149136 manufacture(59779-748)