tums
Generic: calcium carbonate
Labeler: haleon us holdings llcDrug Facts
Product Profile
Brand Name
tums
Generic Name
calcium carbonate
Labeler
haleon us holdings llc
Dosage Form
TABLET
Routes
Active Ingredients
calcium carbonate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0135-0070
Product ID
0135-0070_b826d33d-fb25-442b-8ffa-172acf2b4780
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
2010-03-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01350070
Hyphenated Format
0135-0070
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
tums (source: ndc)
Generic Name
calcium carbonate (source: ndc)
Application Number
M001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 3 PACKAGE in 1 CELLO PACK (0135-0070-03) / 12 TABLET in 1 PACKAGE
- 150 TABLET in 1 BOTTLE (0135-0070-27)
- 12 TABLET in 1 PACKAGE (0135-0070-48)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b826d33d-fb25-442b-8ffa-172acf2b4780", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["210117", "308907"], "spl_set_id": ["35f79dcf-1743-4d9f-aba5-5ead6b056309"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 PACKAGE in 1 CELLO PACK (0135-0070-03) / 12 TABLET in 1 PACKAGE", "package_ndc": "0135-0070-03", "marketing_start_date": "20100310"}, {"sample": false, "description": "150 TABLET in 1 BOTTLE (0135-0070-27)", "package_ndc": "0135-0070-27", "marketing_start_date": "20100310"}, {"sample": false, "description": "12 TABLET in 1 PACKAGE (0135-0070-48)", "package_ndc": "0135-0070-48", "marketing_start_date": "20100310"}], "brand_name": "TUMS", "product_id": "0135-0070_b826d33d-fb25-442b-8ffa-172acf2b4780", "dosage_form": "TABLET", "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": "0135-0070", "generic_name": "calcium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUMS", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100310", "listing_expiration_date": "20261231"}