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OxyRub Pain Relief
OxyRub Pain Relief - 65121-113-04 - (MENTHOL)
Drug Information of OxyRub Pain Relief
| Product NDC: | 65121-113 |
| Proprietary Name: | OxyRub Pain Relief |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 1.25 g/100g & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OxyRub Pain Relief
| Product NDC: | 65121-113 |
| Labeler Name: | Pure Source Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130501 |
Package Information of OxyRub Pain Relief
| Package NDC: | 65121-113-04 |
| Package Description: | 114 g in 1 TUBE (65121-113-04) |
NDC Information of OxyRub Pain Relief
| NDC Code | 65121-113-04 |
| Proprietary Name | OxyRub Pain Relief |
| Package Description | 114 g in 1 TUBE (65121-113-04) |
| Product NDC | 65121-113 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Pure Source Inc. |
| Substance Name | MENTHOL |
| Strength Number | 1.25 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
