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Mentholatum Pain Relief Extra Strength
Mentholatum Pain Relief Extra Strength - 10742-8134-1 - (Menthol)
Drug Information of Mentholatum Pain Relief Extra Strength
| Product NDC: | 10742-8134 |
| Proprietary Name: | Mentholatum Pain Relief Extra Strength |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 30 mg/mL & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mentholatum Pain Relief Extra Strength
| Product NDC: | 10742-8134 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110808 |
Package Information of Mentholatum Pain Relief Extra Strength
| Package NDC: | 10742-8134-1 |
| Package Description: | 236 mL in 1 BOTTLE, PUMP (10742-8134-1) |
NDC Information of Mentholatum Pain Relief Extra Strength
| NDC Code | 10742-8134-1 |
| Proprietary Name | Mentholatum Pain Relief Extra Strength |
| Package Description | 236 mL in 1 BOTTLE, PUMP (10742-8134-1) |
| Product NDC | 10742-8134 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110808 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | MENTHOL |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
