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Benadryl Extra Strength Itch Stopping
Benadryl Extra Strength Itch Stopping - 58232-0744-1 - (Diphenhydramine Hydrochloride)
Drug Information of Benadryl Extra Strength Itch Stopping
| Product NDC: | 58232-0744 |
| Proprietary Name: | Benadryl Extra Strength Itch Stopping |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 20 mg/mL & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benadryl Extra Strength Itch Stopping
| Product NDC: | 58232-0744 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130213 |
Package Information of Benadryl Extra Strength Itch Stopping
| Package NDC: | 58232-0744-1 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (58232-0744-1) |
NDC Information of Benadryl Extra Strength Itch Stopping
| NDC Code | 58232-0744-1 |
| Proprietary Name | Benadryl Extra Strength Itch Stopping |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (58232-0744-1) |
| Product NDC | 58232-0744 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130213 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
