| Product NDC: | 52241-200 |
| Proprietary Name: | Katinko Pain And Itch Relieving |
| Non Proprietary Name: | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
| Active Ingredient(s): | 11; 7.6; 13.5 g/100g; g/100g; g/100g & nbsp; CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OIL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52241-200 |
| Labeler Name: | Greenstone Pharmaceutical H.K. Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100524 |
| Package NDC: | 52241-200-50 |
| Package Description: | 1 BOTTLE in 1 CARTON (52241-200-50) > 50 g in 1 BOTTLE |
| NDC Code | 52241-200-50 |
| Proprietary Name | Katinko Pain And Itch Relieving |
| Package Description | 1 BOTTLE in 1 CARTON (52241-200-50) > 50 g in 1 BOTTLE |
| Product NDC | 52241-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
| Dosage Form Name | OIL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100524 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Greenstone Pharmaceutical H.K. Inc. |
| Substance Name | CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE |
| Strength Number | 11; 7.6; 13.5 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |