uline antacid
Generic: calcium carbonate
Labeler: ulineDrug Facts
Product Profile
Brand Name
uline antacid
Generic Name
calcium carbonate
Labeler
uline
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
calcium carbonate 420 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69790820
Hyphenated Format
69790-820
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 420 mg/1
Packaging
- 50 PACKET in 1 BOX (69790-820-33) / 2 TABLET, CHEWABLE in 1 PACKET
Packages (1)
Ingredients (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"}