| Product NDC: | 50786-003 |
| Proprietary Name: | Valtrum Soothing Topical Analgesic |
| Non Proprietary Name: | camphor, menthol |
| Active Ingredient(s): | 3; 3 mg/100mg; mg/100mg & nbsp; camphor, menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50786-003 |
| Labeler Name: | Drogefar C.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100506 |
| Package NDC: | 50786-003-03 |
| Package Description: | 90151.47 mg in 1 BOTTLE, WITH APPLICATOR (50786-003-03) |
| NDC Code | 50786-003-03 |
| Proprietary Name | Valtrum Soothing Topical Analgesic |
| Package Description | 90151.47 mg in 1 BOTTLE, WITH APPLICATOR (50786-003-03) |
| Product NDC | 50786-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | camphor, menthol |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100506 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Drogefar C.A. |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
| Strength Number | 3; 3 |
| Strength Unit | mg/100mg; mg/100mg |
| Pharmaceutical Classes |