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 |