| 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 |