Home
>
National Drug Code (NDC)
>
LEADER PAIN RELIEVING RUB ULTRA
LEADER PAIN RELIEVING RUB ULTRA - 37205-460-16 - (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE)
Drug Information of LEADER PAIN RELIEVING RUB ULTRA
| Product NDC: | 37205-460 |
| Proprietary Name: | LEADER PAIN RELIEVING RUB ULTRA |
| Non Proprietary Name: | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
| Active Ingredient(s): | 40; 100; 300 mg/g; mg/g; mg/g & nbsp; CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEADER PAIN RELIEVING RUB ULTRA
| Product NDC: | 37205-460 |
| Labeler Name: | CARDINAL HEALTH |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120731 |
Package Information of LEADER PAIN RELIEVING RUB ULTRA
| Package NDC: | 37205-460-16 |
| Package Description: | 1 TUBE in 1 CARTON (37205-460-16) > 57 g in 1 TUBE |
NDC Information of LEADER PAIN RELIEVING RUB ULTRA
| NDC Code | 37205-460-16 |
| Proprietary Name | LEADER PAIN RELIEVING RUB ULTRA |
| Package Description | 1 TUBE in 1 CARTON (37205-460-16) > 57 g in 1 TUBE |
| Product NDC | 37205-460 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120731 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CARDINAL HEALTH |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE |
| Strength Number | 40; 100; 300 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
