Home NDC 69790-089 Uline Antacid
Product NDC 69790-089
11-digit product format 697900089
Labeler code 69790
Product ID 69790-089_debc3184-6bb1-11d1-e053-2995a90af277
Type HUMAN OTC DRUG
Nonproprietary name calcium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Uline
Application part331
Marketing category OTC MONOGRAPH FINAL
Marketing start 2019-10-07
Marketing end 0000-00-00
Substance CALCIUM CARBONATE
Active strength 420 mg/1
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69790-089-33 Uline Antacid 2 in 1 PACKET TABLET, CHEWABLE 2 9 69790-089-33 Uline Antacid 50 in 1 BOX TABLET, CHEWABLE 50 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69790-089 ULINE ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [ULINE] 8 Legacy NDC, 2 package rows 20240127_9014f295-e816-9bcd-e053-2a95a90ae103.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69790-089-33 69790008933 50 PACKET in 1 BOX (69790-089-33) > 2 TABLET, CHEWABLE in 1 PACKET 50 packet 2019-10-07 0000-00-00 No No Current