aluminum hydroxide

Generic: aluminum hydroxide

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name aluminum hydroxide
Generic Name aluminum hydroxide
Labeler atlantic biologicals corp.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

aluminum hydroxide 320 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0091
Product ID 17856-0091_4602216a-bb8c-af52-e063-6294a90a380e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 2005-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178560091
Hyphenated Format 17856-0091

Supplemental Identifiers

RxCUI
308078
UNII
5QB0T2IUN0

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 aluminum hydroxide (source: ndc)
Generic Name aluminum hydroxide (source: ndc)
Application Number M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 320 mg/5mL
source: ndc
Packaging
  • 30 mL in 1 CUP (17856-0091-3)
source: ndc

Packages (1)

17856-0091-3 30 mL in 1 CUP (17856-0091-3)

Ingredients (1)

aluminum hydroxide (320 mg/5mL)

Linked Drug Pages (1)

Aluminum Hydroxide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4602216a-bb8c-af52-e063-6294a90a380e", "openfda": {"unii": ["5QB0T2IUN0"], "rxcui": ["308078"], "spl_set_id": ["60a54d4e-89c2-4329-86bf-a288527f37b5"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 CUP (17856-0091-3)", "package_ndc": "17856-0091-3", "marketing_start_date": "20240416"}], "brand_name": "Aluminum Hydroxide", "product_id": "17856-0091_4602216a-bb8c-af52-e063-6294a90a380e", "dosage_form": "LIQUID", "product_ndc": "17856-0091", "generic_name": "aluminum hydroxide", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aluminum Hydroxide", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "320 mg/5mL"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050201", "listing_expiration_date": "20261231"}