Label: GOOD NEIGHBOR PHARMACY ANTACID REGULAR STRENGTH- calcium carbonate tablet, chewable
- NDC Code(s): 24385-485-47
- Packager: AmerisourceBergen Drug Corporation
- 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.
Updated January 11, 2022
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Active ingredient (in each tablet)
Calcium carbonate 500 mg
- acid indigestion
Ask a doctor or pharmacist before use if you are
- presently taking a prescription drug. Antacids may interact with certain prescription drugs.
When using this product
do not take more than 15 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.
If pregnant or breast feeding,
ask a health professional before use. Keep out of reach of children.
- adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor.
- Good Neighbor Pharmacy Antacid
INGREDIENTS AND APPEARANCE
GOOD NEIGHBOR PHARMACY ANTACID REGULAR STRENGTH
calcium carbonate tablet, chewable
Product Information Product Type HUMAN OTC DRUG Item Code (Source) 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: 2S7830E561) DEXTROSE, UNSPECIFIED FORM (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:24385-485-47 150 in 1 BOTTLE; Type 0: Not a Combination Product 07/13/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 07/13/2010 Labeler - AmerisourceBergen Drug Corporation (007914906) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 manufacture(24385-485) , label(24385-485)