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Celox Ultra - 75990-007-10 - (ALCOHOL)

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Drug Information of Celox Ultra

Product NDC: 75990-007
Proprietary Name: Celox Ultra
Non Proprietary Name: ALCOHOL
Active Ingredient(s): .7    mL/mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Celox Ultra

Product NDC: 75990-007
Labeler Name: Certus Medical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110425

Package Information of Celox Ultra

Package NDC: 75990-007-10
Package Description: 1000 mL in 1 CARTRIDGE (75990-007-10)

NDC Information of Celox Ultra

NDC Code 75990-007-10
Proprietary Name Celox Ultra
Package Description 1000 mL in 1 CARTRIDGE (75990-007-10)
Product NDC 75990-007
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110425
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Certus Medical, Inc.
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Celox Ultra


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