Label: ASSORTED FRUIT PANNED- calcium carbonate tablet, chewable
-
Contains inactivated NDC Code(s)
NDC Code(s): 52642-229-06 - Packager: BestCo Inc
- Category: HUMAN OTC DRUG LABEL
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 February 16, 2016
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR/PHARMACIST
- WHEN USING
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Inactive Ingredients
acacia, carmine, carnauba wax, citric acid, corn starch, corn syrup, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, FD&C yellow #6, flavors, hydrogenated coconut oil, lecithin, medium chain triglycerides, methly paraben, modified starch, phosporic acid, pregelatinized modified starch, propylene glycol, propyl paraben, purified water, shellac, sodium benozate, sorbic acid, sorbitol, sucrose, titanium dioxide, begetable oil, white wax
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ASSORTED FRUIT PANNED
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52642-229 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 CARNAUBA WAX (UNII: R12CBM0EIZ) Product Characteristics Color orange, pink, yellow Score score with uneven pieces Shape ROUND Size 70mm Flavor ORANGE, STRAWBERRY, LEMON Imprint Code AS Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52642-229-06 6 in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 10/01/2014 Labeler - BestCo Inc (002149136) Registrant - Bayer (112117283) Establishment Name Address ID/FEI Business Operations BestCo Inc. 002149136 manufacture(52642-229)