gaviscon

Generic: aluminum hydroxide and magnesium carbonate

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

Drug Facts

Product Profile

Brand Name gaviscon
Generic Name aluminum hydroxide and magnesium carbonate
Labeler haleon us holdings llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

aluminum hydroxide 95 mg/15mL, magnesium carbonate 358 mg/15mL

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0094
Product ID 0135-0094_4aba2043-4dde-0c18-e063-6294a90a5fcf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2027-12-31
Marketing Start 2011-01-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350094
Hyphenated Format 0135-0094

Supplemental Identifiers

RxCUI
245001 252203 404472 1251365
UNII
5QB0T2IUN0 0E53J927NA

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 gaviscon (source: ndc)
Generic Name aluminum hydroxide and magnesium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 95 mg/15mL
  • 358 mg/15mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (0135-0094-41)
  • 177 mL in 1 BOTTLE (0135-0094-42)
source: ndc

Packages (2)

0135-0094-41 355 mL in 1 BOTTLE (0135-0094-41) 0135-0094-42 177 mL in 1 BOTTLE (0135-0094-42)

Ingredients (2)

aluminum hydroxide (95 mg/15mL) magnesium carbonate (358 mg/15mL)

Linked Drug Pages (1)

GAVISCON ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4aba2043-4dde-0c18-e063-6294a90a5fcf", "openfda": {"unii": ["5QB0T2IUN0", "0E53J927NA"], "rxcui": ["245001", "252203", "404472", "1251365"], "spl_set_id": ["2d74e5bc-1f10-4fb6-9258-cd906e360013"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (0135-0094-41)", "package_ndc": "0135-0094-41", "marketing_start_date": "20110114"}, {"sample": false, "description": "177 mL in 1 BOTTLE (0135-0094-42)", "package_ndc": "0135-0094-42", "marketing_start_date": "20110114"}], "brand_name": "GAVISCON", "product_id": "0135-0094_4aba2043-4dde-0c18-e063-6294a90a5fcf", "dosage_form": "LIQUID", "product_ndc": "0135-0094", "generic_name": "aluminum hydroxide and magnesium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GAVISCON", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "95 mg/15mL"}, {"name": "MAGNESIUM CARBONATE", "strength": "358 mg/15mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110114", "listing_expiration_date": "20271231"}