Home
>
National Drug Code (NDC)
>
Atopalm Itch Relief
Atopalm Itch Relief - 51141-4000-1 - (DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE)
Drug Information of Atopalm Itch Relief
| Product NDC: | 51141-4000 |
| Proprietary Name: | Atopalm Itch Relief |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE |
| Active Ingredient(s): | 2; .1 g/100g; g/100g & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Atopalm Itch Relief
| Product NDC: | 51141-4000 |
| Labeler Name: | Neopharm Co, Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110316 |
Package Information of Atopalm Itch Relief
| Package NDC: | 51141-4000-1 |
| Package Description: | 1 TUBE in 1 BOX (51141-4000-1) > 28.3 g in 1 TUBE |
NDC Information of Atopalm Itch Relief
| NDC Code | 51141-4000-1 |
| Proprietary Name | Atopalm Itch Relief |
| Package Description | 1 TUBE in 1 BOX (51141-4000-1) > 28.3 g in 1 TUBE |
| Product NDC | 51141-4000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110316 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Neopharm Co, Ltd |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 2; .1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
