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Dermal Wound Cleanser
Dermal Wound Cleanser - 50484-490-00 - (BENZETHONIUM CHLORIDE)
Drug Information of Dermal Wound Cleanser
| Product NDC: | 50484-490 |
| Proprietary Name: | Dermal Wound Cleanser |
| Non Proprietary Name: | BENZETHONIUM CHLORIDE |
| Active Ingredient(s): | 1.3 uL/mL & nbsp; BENZETHONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dermal Wound Cleanser
| Product NDC: | 50484-490 |
| Labeler Name: | Smith & Nephew, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19910401 |
Package Information of Dermal Wound Cleanser
| Package NDC: | 50484-490-00 |
| Package Description: | 236 mL in 1 BOTTLE, SPRAY (50484-490-00) |
NDC Information of Dermal Wound Cleanser
| NDC Code | 50484-490-00 |
| Proprietary Name | Dermal Wound Cleanser |
| Package Description | 236 mL in 1 BOTTLE, SPRAY (50484-490-00) |
| Product NDC | 50484-490 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZETHONIUM CHLORIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 19910401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Smith & Nephew, Inc. |
| Substance Name | BENZETHONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | uL/mL |
| Pharmaceutical Classes |
