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Lanacane Anti Itch Original Strength - 11509-0302-1 - (benzocaine and benzethonium chloride)

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Drug Information of Lanacane Anti Itch Original Strength

Product NDC: 11509-0302
Proprietary Name: Lanacane Anti Itch Original Strength
Non Proprietary Name: benzocaine and benzethonium chloride
Active Ingredient(s): 2; 60    mg/g; mg/g & nbsp;   benzocaine and benzethonium chloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lanacane Anti Itch Original Strength

Product NDC: 11509-0302
Labeler Name: Combe Incorporated
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19971231

Package Information of Lanacane Anti Itch Original Strength

Package NDC: 11509-0302-1
Package Description: 1 TUBE in 1 CARTON (11509-0302-1) > 74 g in 1 TUBE

NDC Information of Lanacane Anti Itch Original Strength

NDC Code 11509-0302-1
Proprietary Name Lanacane Anti Itch Original Strength
Package Description 1 TUBE in 1 CARTON (11509-0302-1) > 74 g in 1 TUBE
Product NDC 11509-0302
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzocaine and benzethonium chloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19971231
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Combe Incorporated
Substance Name BENZETHONIUM CHLORIDE; BENZOCAINE
Strength Number 2; 60
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of Lanacane Anti Itch Original Strength


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