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ULTRA THERAPY PAIN RELIEF
ULTRA THERAPY PAIN RELIEF - 55628-1001-2 - (MENTHOL, METHYL SALICYLATE, CAPSAICIN)
Drug Information of ULTRA THERAPY PAIN RELIEF
| Product NDC: | 55628-1001 |
| Proprietary Name: | ULTRA THERAPY PAIN RELIEF |
| Non Proprietary Name: | MENTHOL, METHYL SALICYLATE, CAPSAICIN |
| Active Ingredient(s): | .025; 10; 28 g/100mL; g/100mL; g/100mL & nbsp; MENTHOL, METHYL SALICYLATE, CAPSAICIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRA THERAPY PAIN RELIEF
| Product NDC: | 55628-1001 |
| Labeler Name: | Cal Pharma |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121129 |
Package Information of ULTRA THERAPY PAIN RELIEF
| Package NDC: | 55628-1001-2 |
| Package Description: | 120 mL in 1 TUBE (55628-1001-2) |
NDC Information of ULTRA THERAPY PAIN RELIEF
| NDC Code | 55628-1001-2 |
| Proprietary Name | ULTRA THERAPY PAIN RELIEF |
| Package Description | 120 mL in 1 TUBE (55628-1001-2) |
| Product NDC | 55628-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL, METHYL SALICYLATE, CAPSAICIN |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20121129 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cal Pharma |
| Substance Name | CAPSAICIN; MENTHOL; METHYL SALICYLATE |
| Strength Number | .025; 10; 28 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes |
