Product NDC: | 52241-100 |
Proprietary Name: | Katinko Pain And Itch Relieving |
Non Proprietary Name: | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
Active Ingredient(s): | 11; 7.6; 13 g/100g; g/100g; g/100g & nbsp; CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52241-100 |
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: | 52241-100-10 |
Package Description: | 1 JAR in 1 CARTON (52241-100-10) > 10 g in 1 JAR |
NDC Code | 52241-100-10 |
Proprietary Name | Katinko Pain And Itch Relieving |
Package Description | 1 JAR in 1 CARTON (52241-100-10) > 10 g in 1 JAR |
Product NDC | 52241-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE |
Dosage Form Name | OINTMENT |
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 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |