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Ocean Breeze Antibacterial Hand - 43269-667-01 - (ALCOHOL)

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Drug Information of Ocean Breeze Antibacterial Hand

Product NDC: 43269-667
Proprietary Name: Ocean Breeze Antibacterial Hand
Non Proprietary Name: ALCOHOL
Active Ingredient(s): 65    mL/100mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Ocean Breeze Antibacterial Hand

Product NDC: 43269-667
Labeler Name: SJ Creations, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110223

Package Information of Ocean Breeze Antibacterial Hand

Package NDC: 43269-667-01
Package Description: 29 mL in 1 TUBE (43269-667-01)

NDC Information of Ocean Breeze Antibacterial Hand

NDC Code 43269-667-01
Proprietary Name Ocean Breeze Antibacterial Hand
Package Description 29 mL in 1 TUBE (43269-667-01)
Product NDC 43269-667
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110223
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name SJ Creations, Inc.
Substance Name ALCOHOL
Strength Number 65
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Ocean Breeze Antibacterial Hand


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