gaviscon extra strength

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 extra strength
Generic Name aluminum hydroxide and magnesium carbonate
Labeler haleon us holdings llc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

aluminum hydroxide 160 mg/1, magnesium carbonate 105 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0430
Product ID 0135-0430_02f611d3-df31-4514-86ae-9e81004acdbf
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2011-06-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350430
Hyphenated Format 0135-0430

Supplemental Identifiers

RxCUI
212978 308072
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 extra strength (source: ndc)
Generic Name aluminum hydroxide and magnesium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
  • 105 mg/1
source: ndc
Packaging
  • 100 TABLET, CHEWABLE in 1 BOTTLE (0135-0430-03)
source: ndc

Packages (1)

0135-0430-03 100 TABLET, CHEWABLE in 1 BOTTLE (0135-0430-03)

Ingredients (2)

aluminum hydroxide (160 mg/1) magnesium carbonate (105 mg/1)

Linked Drug Pages (1)

Gaviscon Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "02f611d3-df31-4514-86ae-9e81004acdbf", "openfda": {"unii": ["5QB0T2IUN0", "0E53J927NA"], "rxcui": ["212978", "308072"], "spl_set_id": ["7f367927-c366-465c-a059-e2cfb337d562"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (0135-0430-03)", "package_ndc": "0135-0430-03", "marketing_start_date": "20110613"}], "brand_name": "Gaviscon Extra Strength", "product_id": "0135-0430_02f611d3-df31-4514-86ae-9e81004acdbf", "dosage_form": "TABLET, CHEWABLE", "product_ndc": "0135-0430", "generic_name": "aluminum hydroxide and magnesium carbonate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Gaviscon", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "160 mg/1"}, {"name": "MAGNESIUM CARBONATE", "strength": "105 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110613", "listing_expiration_date": "20261231"}