NDC 54162-221

Dermadrox

Aluminum Hydroxide

Dermadrox is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Geritrex Llc. The primary component is Aluminum Hydroxide.

• Product ID: 54162-221_31e3fc58-0d5f-492f-b1f7-2e738c51a7f9
• NDC: 54162-221
• Product Type: Human Otc Drug
• Proprietary Name: Dermadrox
• Generic Name: Aluminum Hydroxide
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-10-15
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part347
• Labeler Name: GERITREX LLC
• Substance Name: ALUMINUM HYDROXIDE
• Active Ingredient Strength: 1 g/113g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 54162-221-01

113 g in 1 TUBE (54162-221-01)

• Marketing Start Date: 2015-07-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54162-221-01 [54162022101]

Dermadrox OINTMENT

• Marketing Category: OTC monograph final
• Application Number: part347
• Product Type: HUMAN OTC DRUG
• Billing Unit: GM
• Marketing Start Date: 2015-07-31
• Inactivation Date: 2020-01-31

NDC 54162-221-04 [54162022104]

Dermadrox OINTMENT

• Marketing Category: OTC monograph final
• Application Number: part347
• Product Type: HUMAN OTC DRUG
• Billing Unit: GM
• Marketing Start Date: 2015-07-31
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ALUMINUM HYDROXIDE	1.356 g/113g

OpenFDA Data

• SPL SET ID: fa0b70c8-50e0-4184-9795-c17739c46630
• Manufacturer:
  • GERITREX LLC
• UNII:
  • 5QB0T2IUN0
• RxNorm Concept Unique ID - RxCUI:
  • 1368022
• UPC Code:
  • 0354162221019

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

NDC	Brand Name	Generic Name
54162-220	Dermadrox	Zinc Acetate
54162-221	Dermadrox	Aluminum Hydroxide
0536-0091	Aluminum Hydroxide	aluminum hydroxide
17856-0091	Aluminum Hydroxide	aluminum hydroxide
24451-091	Aluminum Hydroxide	Aluminum Hydroxide