| Product NDC: | 0904-7760 |
| Proprietary Name: | Clear Anti Itch |
| Non Proprietary Name: | Pramoxine HCl, Zinc acetate |
| Active Ingredient(s): | 10; 1 mg/mL; mg/mL & nbsp; Pramoxine HCl, Zinc acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0904-7760 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19950418 |
| Package NDC: | 0904-7760-21 |
| Package Description: | 177 mL in 1 BOTTLE, PLASTIC (0904-7760-21) |
| NDC Code | 0904-7760-21 |
| Proprietary Name | Clear Anti Itch |
| Package Description | 177 mL in 1 BOTTLE, PLASTIC (0904-7760-21) |
| Product NDC | 0904-7760 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pramoxine HCl, Zinc acetate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19950418 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | PRAMOXINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 10; 1 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |