Home NDC 21130-201 Extra Strength
Product NDC 21130-201
11-digit product format 211300201
Labeler code 21130
Product ID 21130-201_4249c6ae-0e26-afb5-e063-6294a90a6e0a
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler BETTER LIVING BRANDS, LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-30
Substance CALCIUM CARBONATE
Active strength 750 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 Extra Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 750 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 308915 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 21130-201-00 Extra Strength 200 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 200 6 21130-201-96 Extra Strength 96 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 96 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-201 EXTRA STRENGTH (CALCIUM CARBONATE) TABLET, CHEWABLE [BETTER LIVING BRANDS, LLC] 5 Current NDC, Legacy NDC, 2 package rows 20241102_9b311b76-1892-4b74-a07a-8b321436d4a0.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 21130-201-00 21130020100 200 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (21130-201-00) 2020-09-30 0000-00-00 No No Current 21130-201-96 21130020196 96 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (21130-201-96) 2020-09-30 0000-00-00 No No Current