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Itch Relief
Itch Relief - 61010-8300-1 - (diphenhydramine hydrochloride)
Drug Information of Itch Relief
| Product NDC: | 61010-8300 |
| Proprietary Name: | Itch Relief |
| Non Proprietary Name: | diphenhydramine hydrochloride |
| Active Ingredient(s): | 20.3 g/L & nbsp; diphenhydramine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Itch Relief
| Product NDC: | 61010-8300 |
| Labeler Name: | Safetec of America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130502 |
Package Information of Itch Relief
| Package NDC: | 61010-8300-1 |
| Package Description: | .0591 L in 1 BOTTLE, SPRAY (61010-8300-1) |
NDC Information of Itch Relief
| NDC Code | 61010-8300-1 |
| Proprietary Name | Itch Relief |
| Package Description | .0591 L in 1 BOTTLE, SPRAY (61010-8300-1) |
| Product NDC | 61010-8300 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130502 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Safetec of America, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 20.3 |
| Strength Unit | g/L |
| Pharmaceutical Classes |
