heartburn relief

Generic: aluminum hydroxide and magnesium carbonate

Labeler: chain drug marketing association
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name heartburn relief
Generic Name aluminum hydroxide and magnesium carbonate
Labeler chain drug marketing association
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 254 mg/5mL, magnesium carbonate 237.5 mg/5mL

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION

Identifiers & Regulatory

Product NDC 63868-565
Product ID 63868-565_097f7264-6848-61fb-e063-6294a90a3f2f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868565
Hyphenated Format 63868-565

Supplemental Identifiers

RxCUI
245001
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 heartburn relief (source: ndc)
Generic Name aluminum hydroxide and magnesium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 254 mg/5mL
  • 237.5 mg/5mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (63868-565-12)
source: ndc

Packages (1)

63868-565-12 355 mL in 1 BOTTLE (63868-565-12)

Ingredients (2)

aluminum hydroxide (254 mg/5mL) magnesium carbonate (237.5 mg/5mL)

Linked Drug Pages (1)

HEARTBURN RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "097f7264-6848-61fb-e063-6294a90a3f2f", "openfda": {"unii": ["5QB0T2IUN0", "0E53J927NA"], "rxcui": ["245001"], "spl_set_id": ["b4656a2f-a866-5f7a-e053-2995a90ac2c2"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (63868-565-12)", "package_ndc": "63868-565-12", "marketing_start_date": "20191101"}], "brand_name": "HEARTBURN RELIEF", "product_id": "63868-565_097f7264-6848-61fb-e063-6294a90a3f2f", "dosage_form": "SUSPENSION", "product_ndc": "63868-565", "generic_name": "aluminum hydroxide and magnesium carbonate", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HEARTBURN RELIEF", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "254 mg/5mL"}, {"name": "MAGNESIUM CARBONATE", "strength": "237.5 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}