Home NDC 41250-723 Antacid
Product NDC 41250-723
11-digit product format 412500723
Labeler code 41250
Product ID 41250-723_c9f58750-74a3-407c-b070-c42688322d4c
Type HUMAN OTC DRUG
Nonproprietary name Calcium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Meijer Distribution Inc
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-03-14
Substance CALCIUM CARBONATE
Active strength 1000 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 Antacid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 1000 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-723-72 Antacid 72 in 1 BOTTLE TABLET, CHEWABLE 72 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-723 ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [MEIJER DISTRIBUTION INC] 10 Current NDC, Legacy NDC, 1 package rows 20241019_b0e7d321-4a2e-4683-a757-259456410bfc.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 41250-723-72 41250072372 72 TABLET, CHEWABLE in 1 BOTTLE (41250-723-72) 2017-03-14 0000-00-00 No No Current