NDC 54866-002

AVERTEAX

Benzyl Alcohol

AVERTEAX is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Camellix, Llc. The primary component is Benzyl Alcohol.

• Product ID: 54866-002_dea0cd6a-9743-4539-a694-c88cf3543525
• NDC: 54866-002
• Product Type: Human Otc Drug
• Proprietary Name: AVERTEAX
• Generic Name: Benzyl Alcohol
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-01-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Camellix, LLC
• Substance Name: BENZYL ALCOHOL
• Active Ingredient Strength: 10 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 54866-002-01

1 TUBE in 1 PACKAGE (54866-002-01) > 7.4 g in 1 TUBE

• Marketing Start Date: 2014-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54866-002-01 [54866000201]

AVERTEAX CREAM

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-01-01
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
BENZYL ALCOHOL	10 mg/g

OpenFDA Data

• SPL SET ID: f86b5de9-8e44-4d06-890e-75f7e71c79e4
• Manufacturer:
  • Camellix, LLC
• UNII:
  • LKG8494WBH

NDC Crossover Matching brand name "AVERTEAX" or generic name "Benzyl Alcohol"

NDC	Brand Name	Generic Name
54866-001	AVERTEAX	zinc oxide and Cocoa Butter
54866-002	AVERTEAX	Benzyl Alcohol
54866-003	AVERTEAX	zinc oxide and Cocoa Butter
71416-001	Protocoxil	BENZYL ALCOHOL
23594-780	Ulesfia	benzyl alcohol
69202-780	Ulesfia	benzyl alcohol
50486-468	Zilactin	benzyl alcohol
72751-0301	Zilactin	benzyl alcohol