Product NDC: | 10742-8120 |
Proprietary Name: | Mentholatum Pain Relief Muscle Rub |
Non Proprietary Name: | Menthol, Methyl salicylate |
Active Ingredient(s): | 59.1; 128 mg/g; mg/g & nbsp; Menthol, Methyl salicylate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10742-8120 |
Labeler Name: | The Mentholatum Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111003 |
Package NDC: | 10742-8120-1 |
Package Description: | 1 TUBE in 1 CARTON (10742-8120-1) > 35 g in 1 TUBE |
NDC Code | 10742-8120-1 |
Proprietary Name | Mentholatum Pain Relief Muscle Rub |
Package Description | 1 TUBE in 1 CARTON (10742-8120-1) > 35 g in 1 TUBE |
Product NDC | 10742-8120 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Menthol, Methyl salicylate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20111003 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | The Mentholatum Company |
Substance Name | MENTHOL; METHYL SALICYLATE |
Strength Number | 59.1; 128 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |