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Lantiseptic - 12090-0032-4 - (MENTHOL, CALAMINE, ZINC OXIDE)

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Drug Information of Lantiseptic

Product NDC: 12090-0032
Proprietary Name: Lantiseptic
Non Proprietary Name: MENTHOL, CALAMINE, ZINC OXIDE
Active Ingredient(s): 20; 4.5; 180    mg/g; mg/g; mg/g & nbsp;   MENTHOL, CALAMINE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Lantiseptic

Product NDC: 12090-0032
Labeler Name: Summit Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091230

Package Information of Lantiseptic

Package NDC: 12090-0032-4
Package Description: 113 g in 1 TUBE (12090-0032-4)

NDC Information of Lantiseptic

NDC Code 12090-0032-4
Proprietary Name Lantiseptic
Package Description 113 g in 1 TUBE (12090-0032-4)
Product NDC 12090-0032
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MENTHOL, CALAMINE, ZINC OXIDE
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20091230
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Summit Industries, Inc.
Substance Name FERRIC OXIDE RED; MENTHOL; ZINC OXIDE
Strength Number 20; 4.5; 180
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of Lantiseptic


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