Search by Drug Name or NDC

NDC 30142-0108-72 Ultra Strength 1000 mg/1 Details

Ultra Strength 1000 mg/1

Ultra Strength is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by KROGER COMPANY. The primary component is CALCIUM CARBONATE.

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: 30142-0108-72
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	30142-0108
Product ID	30142-108_f18845a1-4a67-4727-bb48-eaaff9d6292f
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	Ultra Strength
Proprietary Name Suffix	Natural Antacid
Non-Proprietary Name	Calcium Carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	1000
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	KROGER COMPANY
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2024-12-31

Package

NDC 30142-0108-72 (30142010872)

Pricing Information	N/A
NDC Package Code	30142-108-72
Billing NDC	30142010872
Package	72 TABLET, CHEWABLE in 1 BOTTLE (30142-108-72)
Marketing Start Date	2019-11-19
NDC Exclude Flag	N