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Diphenhydramine
Diphenhydramine - 40002-004-03 - (Diphenhydramine HCl, Zinc Acetate)
Drug Information of Diphenhydramine
| Product NDC: | 40002-004 |
| Proprietary Name: | Diphenhydramine |
| Non Proprietary Name: | Diphenhydramine HCl, Zinc Acetate |
| Active Ingredient(s): | 2; .1 g/100g; g/100g & nbsp; Diphenhydramine HCl, Zinc Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diphenhydramine
| Product NDC: | 40002-004 |
| Labeler Name: | NexMed (USA), Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110829 |
Package Information of Diphenhydramine
| Package NDC: | 40002-004-03 |
| Package Description: | 1 TUBE in 1 CARTON (40002-004-03) > 28 g in 1 TUBE (40002-004-02) |
NDC Information of Diphenhydramine
| NDC Code | 40002-004-03 |
| Proprietary Name | Diphenhydramine |
| Package Description | 1 TUBE in 1 CARTON (40002-004-03) > 28 g in 1 TUBE (40002-004-02) |
| Product NDC | 40002-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl, Zinc Acetate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110829 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NexMed (USA), Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 2; .1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
