Label: CVS WILD BERRY ANTACID CHEWS- calcium carbonate tablet, chewable
- NDC Code(s): 51316-053-60
- 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 March 15, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR/PHARMACIST
- DO NOT USE
- WHEN USING
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients: Beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup, dextrin, ethyl acetate, FD&C blue no. 1 aluminum lake, FD&C blue no. 2 aluminum lake, FD&C red no. 40, FD&C red no. 40 aluminum lake, FD&C yellow no. 5 aluminum lake, FD&C yellow no. 6 aluminum lake, gum arabic, hydrogenated coconut oil, maltodextrin, medium chain triglycerides, modified corn starch, natural and artificial flavors, phosphoric acid, pregelatinized corn starch, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, soybean oil, sucrose and titanium dioxide.
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INGREDIENTS AND APPEARANCE
CVS WILD BERRY ANTACID CHEWS
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51316-053 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 (Pink, Purple, Red) Score no score Shape ROUND Size 14mm Flavor CHERRY (Cherry, Mixed Berry, Strawberry) Imprint Code FC Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51316-053-60 60 in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 03/15/2023 Labeler - CVS Pharmacy (062312574) Registrant - Bestco LLC (002149136) Establishment Name Address ID/FEI Business Operations Bestco LLC 002149136 manufacture(51316-053)