NDC 50486-468

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 Blairex Laboratories, Inc.. The primary component is Benzyl Alcohol.

• Product ID: 50486-468_971e4a73-b1e5-4145-a7e2-8d63837981d0
• NDC: 50486-468
• 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 FINAL
• Application Number: part356
• Labeler Name: Blairex Laboratories, Inc.
• Substance Name: BENZYL ALCOHOL
• Active Ingredient Strength: 0 g/g
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 50486-468-02

1 TUBE in 1 CARTON (50486-468-02) > 7.1 g in 1 TUBE

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

NDC SPL Data Element Entries

NDC 50486-468-02 [50486046802]

Zilactin Early Relief Cold Sore GEL

• Marketing Category: OTC monograph final
• Application Number: part346
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-06-30

Drug Details

Active Ingredients

Ingredient	Strength
BENZYL ALCOHOL	.1 g/g

OpenFDA Data

• SPL SET ID: 0910d0d8-dc69-43bb-967d-08cab8ae917b
• Manufacturer:
  • Blairex Laboratories, Inc.
• UNII:
  • LKG8494WBH
• RxNorm Concept Unique ID - RxCUI:
  • 866357
  • 581456
• UPC Code:
  • 0350486468024

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