NDC 17856-0091

Aluminum Hydroxide

Aluminum Hydroxide

Aluminum Hydroxide is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Atlantic Biologicals Corps. The primary component is Aluminum Hydroxide.

• Product ID: 17856-0091_b70c38bd-125a-4971-b79e-542de98ae936
• NDC: 17856-0091
• Product Type: Human Otc Drug
• Proprietary Name: Aluminum Hydroxide
• Generic Name: Aluminum Hydroxide
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2005-02-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part331
• Labeler Name: Atlantic Biologicals Corps
• Substance Name: ALUMINUM HYDROXIDE
• Active Ingredient Strength: 320 mg/5mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 17856-0091-3

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

• Marketing Start Date: 2021-01-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17856-0091-3 [17856009103]

Aluminum Hydroxide LIQUID

• Marketing Category: OTC monograph final
• Application Number: part331
• Product Type: HUMAN OTC DRUG
• Billing Unit: ML
• Marketing Start Date: 2019-09-16

Drug Details

Active Ingredients

Ingredient	Strength
ALUMINUM HYDROXIDE	320 mg/5mL

OpenFDA Data

• SPL SET ID: 60a54d4e-89c2-4329-86bf-a288527f37b5
• Manufacturer:
  • Atlantic Biologicals Corps
• UNII:
  • 5QB0T2IUN0
• RxNorm Concept Unique ID - RxCUI:
  • 308078

NDC Crossover Matching brand name "Aluminum Hydroxide" or generic name "Aluminum Hydroxide"

NDC	Brand Name	Generic Name
0536-0091	Aluminum Hydroxide	aluminum hydroxide
17856-0091	Aluminum Hydroxide	aluminum hydroxide
24451-091	Aluminum Hydroxide	Aluminum Hydroxide
54162-221	Dermadrox	Aluminum Hydroxide