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Bite and Itch
Bite and Itch - 11383-193-04 - (Diphenhydramine HCl and Pramoxine HCl)
Drug Information of Bite and Itch
| Product NDC: | 11383-193 |
| Proprietary Name: | Bite and Itch |
| Non Proprietary Name: | Diphenhydramine HCl and Pramoxine HCl |
| Active Ingredient(s): | 20; 10 mg/g; mg/g & nbsp; Diphenhydramine HCl and Pramoxine HCl |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bite and Itch
| Product NDC: | 11383-193 |
| Labeler Name: | Weeks & Leo Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20000106 |
Package Information of Bite and Itch
| Package NDC: | 11383-193-04 |
| Package Description: | 113 g in 1 BOTTLE (11383-193-04) |
NDC Information of Bite and Itch
| NDC Code | 11383-193-04 |
| Proprietary Name | Bite and Itch |
| Package Description | 113 g in 1 BOTTLE (11383-193-04) |
| Product NDC | 11383-193 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl and Pramoxine HCl |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20000106 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Weeks & Leo Co., Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 20; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
