Label: ANTACID PEPPERMINT FLAVOUR REGULAR STRENGTH- calcium carbonate tablet, chewable
- NDC Code(s): 68084-988-32, 68084-988-33
- Packager: American Health Packaging
- This is a repackaged label.
- Source NDC Code(s): 24385-485
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 21, 2024
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- Official Label (Printer Friendly)
- Active Ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
Ask a doctor or pharmacist before use if you are
- presently taking a prescription drug. Antacids may interact with certain prescription drugs.
- Directions
- Other Information
- Inactive ingredients
- Packaging Information
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Package/Label Display Panel — Carton — 500 mg
NDC 68084- 988-32
Antacid
Peppermint Flavor
Regular StrengthCalcium Carbonate 500 mg
20 Chewable Tablets (5 x 4)
The drug product contained in this package is from
NDC # 24385-485, AmerisourceBergen distributed for
Good Neighbor Pharmacy ®.Distributed by:
American Health Packaging
2550 John Glenn Avenue, Suite A
Columbus, OH 43217098832
0298832/0322 - Package/Label Display Panel — Blister — 500 mg
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INGREDIENTS AND APPEARANCE
ANTACID PEPPERMINT FLAVOUR REGULAR STRENGTH
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68084-988(NDC:24385-485) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 500 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) CROSPOVIDONE (UNII: 68401960MK) DEXTROSE (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color white Score no score Shape ROUND Size 16mm Flavor PEPPERMINT Imprint Code G;113 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68084-988-32 20 in 1 BOX, UNIT-DOSE 11/16/2015 1 NDC:68084-988-33 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 11/16/2015 Labeler - American Health Packaging (929561009) Establishment Name Address ID/FEI Business Operations American Health Packaging 929561009 repack(68084-988)