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Jock Itch
Jock Itch - 11822-0504-1 - (Clotrimazole)
Drug Information of Jock Itch
| Product NDC: | 11822-0504 |
| Proprietary Name: | Jock Itch |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | 1 g/100g & nbsp; Clotrimazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Jock Itch
| Product NDC: | 11822-0504 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20050807 |
Package Information of Jock Itch
| Package NDC: | 11822-0504-1 |
| Package Description: | 1 TUBE in 1 CARTON (11822-0504-1) > 14 g in 1 TUBE |
NDC Information of Jock Itch
| NDC Code | 11822-0504-1 |
| Proprietary Name | Jock Itch |
| Package Description | 1 TUBE in 1 CARTON (11822-0504-1) > 14 g in 1 TUBE |
| Product NDC | 11822-0504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20050807 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rite Aid Corporation |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
