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RevitaDERM Wound Care
RevitaDERM Wound Care - 63347-120-01 - (BENZALKONIUM CHLORIDE)
Drug Information of RevitaDERM Wound Care
| Product NDC: | 63347-120 |
| Proprietary Name: | RevitaDERM Wound Care |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | 170 mg/89mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RevitaDERM Wound Care
| Product NDC: | 63347-120 |
| Labeler Name: | Blaine Labs Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120524 |
Package Information of RevitaDERM Wound Care
| Package NDC: | 63347-120-01 |
| Package Description: | 89 mL in 1 TUBE (63347-120-01) |
NDC Information of RevitaDERM Wound Care
| NDC Code | 63347-120-01 |
| Proprietary Name | RevitaDERM Wound Care |
| Package Description | 89 mL in 1 TUBE (63347-120-01) |
| Product NDC | 63347-120 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120524 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Blaine Labs Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 170 |
| Strength Unit | mg/89mL |
| Pharmaceutical Classes |
