NDC 72751-0301

Zilactin Early Relief Cold Sore

Benzyl Alcohol

Zilactin Early Relief Cold Sore is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Applied Laboratories, Inc.. The primary component is Benzyl Alcohol.

• Product ID: 72751-0301_d21c275e-697d-e95e-e053-2a95a90ad633
• NDC: 72751-0301
• Product Type: Human Otc Drug
• Proprietary Name: Zilactin Early Relief Cold Sore
• Generic Name: Benzyl Alcohol
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2005-06-30
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Applied Laboratories, Inc.
• Substance Name: BENZYL ALCOHOL
• Active Ingredient Strength: 0 g/g
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 72751-0301-1

1 TUBE in 1 CARTON (72751-0301-1) > 7.1 g in 1 TUBE

• Marketing Start Date: 2005-06-30
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Zilactin Early Relief Cold Sore" or generic name "Benzyl Alcohol"

NDC	Brand Name	Generic Name
54866-002	AVERTEAX	Benzyl Alcohol
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