Home NDC 76162-131 Topcare Ultra Strength Antacid Peppermint
Product NDC 76162-131
11-digit product format 761620131
Labeler code 76162
Product ID 76162-131_47a0f780-1d28-4d5c-8344-f29fad84309d
Type HUMAN OTC DRUG
Nonproprietary name Calcium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Topco Associates, LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-04-25
Substance CALCIUM CARBONATE
Active strength 1000 mg/1
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Topcare Ultra Strength Antacid Peppermint
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308892 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76162-131-68 Topcare Ultra Strength Antacid Peppermint 72 in 1 BOTTLE TABLET, CHEWABLE 72 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76162-131 TOPCARE ULTRA STRENGTH ANTACID PEPPERMINT (CALCIUM CARBONATE) TABLET, CHEWABLE [TOPCO ASSOCIATES, LLC] 2 Current NDC, Legacy NDC, 1 package rows 20241213_fb434059-7b6e-42e0-acfa-db9879f6a4e4.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 10 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 76162-131-68 76162013168 72 TABLET, CHEWABLE in 1 BOTTLE (76162-131-68) 2022-04-25 0000-00-00 No No Current