uline antacid

Generic: calcium carbonate

Labeler: uline
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name uline antacid
Generic Name calcium carbonate
Labeler uline
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 420 mg/1

Manufacturer
Uline

Identifiers & Regulatory

Product NDC 69790-820
Product ID 69790-820_3e4c0f0f-30c8-6e2b-e063-6294a90accbc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-10-07

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69790820
Hyphenated Format 69790-820

Supplemental Identifiers

RxCUI
313884
UNII
H0G9379FGK

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name uline antacid (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 420 mg/1
source: ndc
Packaging
  • 50 PACKET in 1 BOX (69790-820-33) / 2 TABLET, CHEWABLE in 1 PACKET
source: ndc

Packages (1)

Ingredients (1)

calcium carbonate (420 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e4c0f0f-30c8-6e2b-e063-6294a90accbc", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["313884"], "spl_set_id": ["9014f295-e816-9bcd-e053-2a95a90ae103"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (69790-820-33)  / 2 TABLET, CHEWABLE in 1 PACKET", "package_ndc": "69790-820-33", "marketing_start_date": "20191007"}], "brand_name": "Uline Antacid", "product_id": "69790-820_3e4c0f0f-30c8-6e2b-e063-6294a90accbc", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "69790-820", "generic_name": "calcium carbonate", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Uline Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "420 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191007", "listing_expiration_date": "20261231"}