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Derma-Glove
Derma-Glove - 24673-249-06 - (Ethanol, Triclosan)
Drug Information of Derma-Glove
| Product NDC: | 24673-249 |
| Proprietary Name: | Derma-Glove |
| Non Proprietary Name: | Ethanol, Triclosan |
| Active Ingredient(s): | .58; .003 g/g; g/g & nbsp; Ethanol, Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Derma-Glove
| Product NDC: | 24673-249 |
| Labeler Name: | RWM TECHNOLOGIES |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100203 |
Package Information of Derma-Glove
| Package NDC: | 24673-249-06 |
| Package Description: | 1223040 g in 1 DRUM (24673-249-06) |
NDC Information of Derma-Glove
| NDC Code | 24673-249-06 |
| Proprietary Name | Derma-Glove |
| Package Description | 1223040 g in 1 DRUM (24673-249-06) |
| Product NDC | 24673-249 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethanol, Triclosan |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100203 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | RWM TECHNOLOGIES |
| Substance Name | ETHANOL; TRICLOSAN |
| Strength Number | .58; .003 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
