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