tums ultra

Generic: calcium carbonate

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tums ultra
Generic Name calcium carbonate
Labeler haleon us holdings llc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0180
Product ID 0135-0180_35c4dd66-0a1f-dda3-e063-6394a90a2c78
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2010-02-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350180
Hyphenated Format 0135-0180

Supplemental Identifiers

RxCUI
308892 1044524
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 tums ultra (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 86 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-01)
  • 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-02)
  • 160 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-14)
source: ndc

Packages (3)

0135-0180-01 86 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-01) 0135-0180-02 72 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-02) 0135-0180-14 160 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-14)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

TUMS ULTRA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35c4dd66-0a1f-dda3-e063-6394a90a2c78", "openfda": {"unii": ["H0G9379FGK"], "rxcui": ["308892", "1044524"], "spl_set_id": ["f4786707-a0f7-4ba8-9656-06278d1b4b6c"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "86 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-01)", "package_ndc": "0135-0180-01", "marketing_start_date": "20100212"}, {"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-02)", "package_ndc": "0135-0180-02", "marketing_start_date": "20100212"}, {"sample": false, "description": "160 TABLET, CHEWABLE in 1 BOTTLE (0135-0180-14)", "package_ndc": "0135-0180-14", "marketing_start_date": "20100212"}], "brand_name": "TUMS ULTRA", "product_id": "0135-0180_35c4dd66-0a1f-dda3-e063-6394a90a2c78", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0135-0180", "generic_name": "calcium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TUMS", "brand_name_suffix": "ULTRA", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20100212", "listing_expiration_date": "20261231"}