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InstantFOAM non-alcohol - 11084-058-05 - (BENZALKONIUM CHLORIDE)

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Drug Information of InstantFOAM non-alcohol

Product NDC: 11084-058
Proprietary Name: InstantFOAM non-alcohol
Non Proprietary Name: BENZALKONIUM CHLORIDE
Active Ingredient(s): .13    mL/100mL & nbsp;   BENZALKONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of InstantFOAM non-alcohol

Product NDC: 11084-058
Labeler Name: Deb USA, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100101

Package Information of InstantFOAM non-alcohol

Package NDC: 11084-058-05
Package Description: 3780 mL in 1 BOTTLE, PLASTIC (11084-058-05)

NDC Information of InstantFOAM non-alcohol

NDC Code 11084-058-05
Proprietary Name InstantFOAM non-alcohol
Package Description 3780 mL in 1 BOTTLE, PLASTIC (11084-058-05)
Product NDC 11084-058
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZALKONIUM CHLORIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Deb USA, Inc.
Substance Name BENZALKONIUM CHLORIDE
Strength Number .13
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of InstantFOAM non-alcohol


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