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Itch Relief
Itch Relief - 55910-295-16 - (Diphenhydramine HCl, Zinc Acetate)
Drug Information of Itch Relief
| Product NDC: | 55910-295 |
| Proprietary Name: | Itch Relief |
| Non Proprietary Name: | Diphenhydramine HCl, Zinc Acetate |
| Active Ingredient(s): | 2; .1 kg/100L; kg/100L & nbsp; Diphenhydramine HCl, Zinc Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Itch Relief
| Product NDC: | 55910-295 |
| Labeler Name: | DOLGENCORP, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100714 |
Package Information of Itch Relief
| Package NDC: | 55910-295-16 |
| Package Description: | .059 L in 1 BOTTLE, SPRAY (55910-295-16) |
NDC Information of Itch Relief
| NDC Code | 55910-295-16 |
| Proprietary Name | Itch Relief |
| Package Description | .059 L in 1 BOTTLE, SPRAY (55910-295-16) |
| Product NDC | 55910-295 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl, Zinc Acetate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100714 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DOLGENCORP, LLC |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 2; .1 |
| Strength Unit | kg/100L; kg/100L |
| Pharmaceutical Classes |
