Label: ANTACID FLAVOR CHEW- calcium carbonate tablet, chewable
- NDC Code(s): 52642-034-90
- Packager: BestCo Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
-
ASK DOCTOR
Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain perscription drugs.
Do not take more than 5 chews in a 24-hour period, or use the maximum dosage for more than 2 weeks, except udner the advice and supervision of a physician.
When using this product constipation may occur.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Inactive ingredients
Beeswax, carmine, carnauba wax, citric acid, corn starch, 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, phosphoric acid, pregelatinized corn starch, proply paraben, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, soybean oil, sucorse and titanium dioxide.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ANTACID FLAVOR CHEW
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52642-034 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, yellow Score score with uneven pieces Shape ROUND Size 14mm Flavor STRAWBERRY, LEMON, ORANGE Imprint Code FC Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52642-034-90 90 in 1 BOTTLE; Type 0: Not a Combination Product 07/26/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 07/26/2017 Labeler - BestCo Inc. (002149136) Registrant - BestCo Inc. (002149136) Establishment Name Address ID/FEI Business Operations BestCo Inc. 002149136 manufacture(52642-034)