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up and up pain relief
up and up pain relief - 11673-136-01 - (menthol, methyl salicylate)
Drug Information of up and up pain relief
| Product NDC: | 11673-136 |
| Proprietary Name: | up and up pain relief |
| Non Proprietary Name: | menthol, methyl salicylate |
| Active Ingredient(s): | 100; 300 mg/g; mg/g & nbsp; menthol, methyl salicylate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of up and up pain relief
| Product NDC: | 11673-136 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080514 |
Package Information of up and up pain relief
| Package NDC: | 11673-136-01 |
| Package Description: | 1 TUBE in 1 CARTON (11673-136-01) > 85 g in 1 TUBE |
NDC Information of up and up pain relief
| NDC Code | 11673-136-01 |
| Proprietary Name | up and up pain relief |
| Package Description | 1 TUBE in 1 CARTON (11673-136-01) > 85 g in 1 TUBE |
| Product NDC | 11673-136 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | menthol, methyl salicylate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080514 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Target Corporation |
| Substance Name | MENTHOL; METHYL SALICYLATE |
| Strength Number | 100; 300 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
