Home NDC 11673-813 ultra strength antacid
Product NDC 11673-813
11-digit product format 116730813
Labeler code 11673
Product ID 11673-813_42c22d07-2b8a-a3c3-e063-6394a90a687a
Type HUMAN OTC DRUG
Nonproprietary name Calciium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Target Corporation
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-03-15
Substance CALCIUM CARBONATE
Active strength 1000 mg/1
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 ultra strength antacid
Brand name suffix Peppermint Flavored
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-813-47 ultra strength antacidPeppermint Flavored 160 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 160 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-813 ULTRA STRENGTH ANTACID PEPPERMINT FLAVORED (CALCIIUM CARBONATE) TABLET, CHEWABLE [TARGET CORPORATION] 7 Current NDC, Legacy NDC, 1 package rows 20241109_55dc1614-8fc0-4f2c-abfc-b675173b4f07.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 8 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 11673-813-47 11673081347 160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-813-47) 2018-03-15 0000-00-00 No No Current