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Banophen
Banophen - 0904-5354-31 - (Diphenhydramine Hydrochloride, Zinc Acetate)
Drug Information of Banophen
| Product NDC: | 0904-5354 |
| Proprietary Name: | Banophen |
| 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 Banophen
| Product NDC: | 0904-5354 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090619 |
Package Information of Banophen
| Package NDC: | 0904-5354-31 |
| Package Description: | 1 TUBE in 1 CARTON (0904-5354-31) > 28 g in 1 TUBE |
NDC Information of Banophen
| NDC Code | 0904-5354-31 |
| Proprietary Name | Banophen |
| Package Description | 1 TUBE in 1 CARTON (0904-5354-31) > 28 g in 1 TUBE |
| Product NDC | 0904-5354 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride, Zinc Acetate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090619 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
| Strength Number | 2; .1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
