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Lantiseptic - 12090-0019-1 - (LANOLIN)

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Drug Information of Lantiseptic

Product NDC: 12090-0019
Proprietary Name: Lantiseptic
Non Proprietary Name: LANOLIN
Active Ingredient(s): 500    mg/g & nbsp;   LANOLIN
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lantiseptic

Product NDC: 12090-0019
Labeler Name: Summit Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20091230

Package Information of Lantiseptic

Package NDC: 12090-0019-1
Package Description: 14.2 g in 1 JAR (12090-0019-1)

NDC Information of Lantiseptic

NDC Code 12090-0019-1
Proprietary Name Lantiseptic
Package Description 14.2 g in 1 JAR (12090-0019-1)
Product NDC 12090-0019
Product Type Name HUMAN OTC DRUG
Non Proprietary Name LANOLIN
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20091230
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Summit Industries, Inc.
Substance Name LANOLIN
Strength Number 500
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Lantiseptic


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