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Dermal Wound Cleanser - 50484-492-00 - (BENZETHONIUM CHLORIDE)

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Drug Information of Dermal Wound Cleanser

Product NDC: 50484-492
Proprietary Name: Dermal Wound Cleanser
Non Proprietary Name: BENZETHONIUM CHLORIDE
Active Ingredient(s): 1.3    uL/mL & nbsp;   BENZETHONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Dermal Wound Cleanser

Product NDC: 50484-492
Labeler Name: Smith & Nephew, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19940401

Package Information of Dermal Wound Cleanser

Package NDC: 50484-492-00
Package Description: 473 mL in 1 BOTTLE, SPRAY (50484-492-00)

NDC Information of Dermal Wound Cleanser

NDC Code 50484-492-00
Proprietary Name Dermal Wound Cleanser
Package Description 473 mL in 1 BOTTLE, SPRAY (50484-492-00)
Product NDC 50484-492
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZETHONIUM CHLORIDE
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 19940401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Smith & Nephew, Inc.
Substance Name BENZETHONIUM CHLORIDE
Strength Number 1.3
Strength Unit uL/mL
Pharmaceutical Classes

Complete Information of Dermal Wound Cleanser


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