NDC 24451-091

Aluminum Hydroxide

Aluminum Hydroxide

Aluminum Hydroxide is a Oral Gel in the Human Otc Drug category. It is labeled and distributed by Llc Federal Solutions. The primary component is Aluminum Hydroxide.

• Product ID: 24451-091_18de8a4b-df09-498a-ab6b-df914a59e48a
• NDC: 24451-091
• Product Type: Human Otc Drug
• Proprietary Name: Aluminum Hydroxide
• Generic Name: Aluminum Hydroxide
• Dosage Form: Gel
• Route of Administration: ORAL
• Marketing Start Date: 2013-08-12
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part331
• Labeler Name: LLC Federal Solutions
• Substance Name: ALUMINUM HYDROXIDE
• Active Ingredient Strength: 320 mg/5mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 24451-091-30

100 CUP, UNIT-DOSE in 1 BOX (24451-091-30) > 30 mL in 1 CUP, UNIT-DOSE

• Marketing Start Date: 2013-08-12
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 24451-091-30 [24451009130]

Aluminum Hydroxide GEL

• Marketing Category: OTC monograph final
• Application Number: part331
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-08-12
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
ALUMINUM HYDROXIDE	320 mg/5mL

OpenFDA Data

• SPL SET ID: af9b799f-69c5-401c-9c43-a97b23384cc2
• Manufacturer:
  • LLC Federal Solutions
• 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