Label: ANTACID FRUIT CHEW- calcium carbonate tablet, chewable
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Contains inactivated NDC Code(s)
NDC Code(s): 69842-361-50 - 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 10, 2017
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR/PHARMACIST
- WHEN USING
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients: Beeswax, calcium carbonate, carnauba wax, coconut oil, corn syrup, ethyl acetate, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, FD&C yellow no. 5 aluminum lake, FD&C yellow no. 6, FD&C yellow no. 6 aluminum lake, gum arabic, medium chain triclycerides, methyl paraben, modified corn starch, modified potato starch, natural and artificial flavors, palm oil, phosphoric acid, polyvinylpyrrolidone, potassium sorbate, propyl paraben, saccharose, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, and water.
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INGREDIENTS AND APPEARANCE
ANTACID FRUIT CHEW
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-361 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 1000 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color green (Green, Orange, Red) Score no score Shape ROUND Size 14mm Flavor CHERRY (Cherry, Lime, Orange) Imprint Code FC Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-361-50 50 in 1 BOTTLE; Type 0: Not a Combination Product 01/31/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 01/31/2017 Labeler - CVS Pharmacy (062312574) Registrant - Bestco Inc. (002149136) Establishment Name Address ID/FEI Business Operations Bestco Inc. 002149136 manufacture(69842-361)