Product NDC: | 0869-0218 |
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: | 0869-0218 |
Labeler Name: | /Vi-Jon |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19940507 |
Package NDC: | 0869-0218-30 |
Package Description: | 177 mL in 1 BOTTLE, PLASTIC (0869-0218-30) |
NDC Code | 0869-0218-30 |
Proprietary Name | Clear Anti Itch |
Package Description | 177 mL in 1 BOTTLE, PLASTIC (0869-0218-30) |
Product NDC | 0869-0218 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Pramoxine HCl, Zinc acetate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 19940507 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | /Vi-Jon |
Substance Name | PRAMOXINE HYDROCHLORIDE; ZINC ACETATE |
Strength Number | 10; 1 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |