Home > National Drug Code (NDC) > Vagisil Anti Itch Original Strength

Vagisil Anti Itch Original Strength - 11509-0360-1 - (Benzocaine and Resorcinol)

Alphabetical Index


Drug Information of Vagisil Anti Itch Original Strength

Product NDC: 11509-0360
Proprietary Name: Vagisil Anti Itch Original Strength
Non Proprietary Name: Benzocaine and Resorcinol
Active Ingredient(s): 50; 20    mg/g; mg/g & nbsp;   Benzocaine and Resorcinol
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Vagisil Anti Itch Original Strength

Product NDC: 11509-0360
Labeler Name: Combe Incorporated
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19740801

Package Information of Vagisil Anti Itch Original Strength

Package NDC: 11509-0360-1
Package Description: 1 TUBE in 1 CARTON (11509-0360-1) > 28 g in 1 TUBE

NDC Information of Vagisil Anti Itch Original Strength

NDC Code 11509-0360-1
Proprietary Name Vagisil Anti Itch Original Strength
Package Description 1 TUBE in 1 CARTON (11509-0360-1) > 28 g in 1 TUBE
Product NDC 11509-0360
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzocaine and Resorcinol
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19740801
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Combe Incorporated
Substance Name BENZOCAINE; RESORCINOL
Strength Number 50; 20
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of Vagisil Anti Itch Original Strength


General Information