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Natralia Anti Fungal - 43251-3361-1 - (Undecylenic acid)

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Drug Information of Natralia Anti Fungal

Product NDC: 43251-3361
Proprietary Name: Natralia Anti Fungal
Non Proprietary Name: Undecylenic acid
Active Ingredient(s): 250    mg/mL & nbsp;   Undecylenic acid
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Natralia Anti Fungal

Product NDC: 43251-3361
Labeler Name: Laderma Trading Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: part333C
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090103

Package Information of Natralia Anti Fungal

Package NDC: 43251-3361-1
Package Description: 1 BOTTLE in 1 CARTON (43251-3361-1) > 30 mL in 1 BOTTLE

NDC Information of Natralia Anti Fungal

NDC Code 43251-3361-1
Proprietary Name Natralia Anti Fungal
Package Description 1 BOTTLE in 1 CARTON (43251-3361-1) > 30 mL in 1 BOTTLE
Product NDC 43251-3361
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Undecylenic acid
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20090103
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Laderma Trading Pty Ltd
Substance Name UNDECYLENIC ACID
Strength Number 250
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Natralia Anti Fungal


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