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Recens Ultra - 75990-365-10 - (ALCOHOL)

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Drug Information of Recens Ultra

Product NDC: 75990-365
Proprietary Name: Recens Ultra
Non Proprietary Name: ALCOHOL
Active Ingredient(s): .7    mL/mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Recens Ultra

Product NDC: 75990-365
Labeler Name: Certus Medical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110728

Package Information of Recens Ultra

Package NDC: 75990-365-10
Package Description: 1000 mL in 1 CARTRIDGE (75990-365-10)

NDC Information of Recens Ultra

NDC Code 75990-365-10
Proprietary Name Recens Ultra
Package Description 1000 mL in 1 CARTRIDGE (75990-365-10)
Product NDC 75990-365
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110728
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 Recens Ultra


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