| Product NDC: | 10742-8157 |
| Proprietary Name: | Mentholatum Ironman |
| Non Proprietary Name: | Camphor, Menthol |
| Active Ingredient(s): | 30; 40 mg/g; mg/g & nbsp; Camphor, Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10742-8157 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100201 |
| Package NDC: | 10742-8157-1 |
| Package Description: | 1 TUBE in 1 CARTON (10742-8157-1) > 85 g in 1 TUBE |
| NDC Code | 10742-8157-1 |
| Proprietary Name | Mentholatum Ironman |
| Package Description | 1 TUBE in 1 CARTON (10742-8157-1) > 85 g in 1 TUBE |
| Product NDC | 10742-8157 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Camphor, Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
| Strength Number | 30; 40 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |