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NDC 30142-0039-32 Antacid - Anti-Gas Relief 750; 80 mg/1; mg/1 Details

Antacid - Anti-Gas Relief 750; 80 mg/1; mg/1

Antacid - Anti-Gas Relief is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Kroger. The primary component is CALCIUM CARBONATE; DIMETHICONE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 30142-0039-32
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Simethicone is used to treat the symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 30142-0039-32
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Simethicone

Product Information

NDC	30142-0039
Product ID	30142-039_08a201f2-64ad-552e-e063-6394a90a0686
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Antacid - Anti-Gas Relief
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	750; 80
Active Ingredient Units	mg/1; mg/1
Substance Name	CALCIUM CARBONATE; DIMETHICONE
Labeler Name	Kroger
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Skin Barrier Activity [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M001
Listing Certified Through	2024-12-31

Package

NDC 30142-0039-32 (30142003932)

Pricing Information	N/A
NDC Package Code	30142-039-32
Billing NDC	30142003932
Package	32 TABLET, CHEWABLE in 1 BOTTLE (30142-039-32)
Marketing Start Date	2019-01-28
NDC Exclude Flag	N