Home NDC 41163-171 EQU Ultra Strength Antacid Assorted Fruit 171AF
Product NDC 41163-171
11-digit product format 411630171
Labeler code 41163
Product ID 41163-171_8cfe3fe3-99fa-44ae-a68e-8c8e97e23177
Type HUMAN OTC DRUG
Nonproprietary name Calcium carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler UNITED NATURAL FOODS, INC. DBA UNFI
Application part331
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-12
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 Additional Listing Data#
Finished product Yes
Brand name base EQU Ultra Strength Antacid Assorted Fruit 171AF
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 41163-171-68 EQU Ultra Strength Antacid Assorted Fruit 171AF 72 in 1 BOTTLE TABLET, CHEWABLE 72 1 41163-171-75 EQU Ultra Strength Antacid Assorted Fruit 171AF 160 in 1 BOTTLE TABLET, CHEWABLE 160 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41163-171 EQU ULTRA STRENGTH ANTACID ASSORTED FRUIT 171AF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNITED NATURAL FOODS, INC. DBA UNFI] 1 Current NDC, 2 package rows 20240513_8cfe3fe3-99fa-44ae-a68e-8c8e97e23177.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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 41163-171-68 41163017168 72 TABLET, CHEWABLE in 1 BOTTLE (41163-171-68) 2024-05-12 No No Current 41163-171-75 41163017175 160 TABLET, CHEWABLE in 1 BOTTLE (41163-171-75) 2024-05-12 No No Current