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Preventage Hand Treatment
Preventage Hand Treatment - 57627-109-01 - (OCTINOXATE,OXYBENZONE)
Drug Information of Preventage Hand Treatment
| Product NDC: | 57627-109 |
| Proprietary Name: | Preventage Hand Treatment |
| Non Proprietary Name: | OCTINOXATE,OXYBENZONE |
| Active Ingredient(s): | 4; 2 g/100g; g/100g & nbsp; OCTINOXATE,OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Preventage Hand Treatment
| Product NDC: | 57627-109 |
| Labeler Name: | Merle Norman Cosmetics, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110423 |
Package Information of Preventage Hand Treatment
| Package NDC: | 57627-109-01 |
| Package Description: | 113 g in 1 TUBE (57627-109-01) |
NDC Information of Preventage Hand Treatment
| NDC Code | 57627-109-01 |
| Proprietary Name | Preventage Hand Treatment |
| Package Description | 113 g in 1 TUBE (57627-109-01) |
| Product NDC | 57627-109 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE,OXYBENZONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110423 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Merle Norman Cosmetics, Inc |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 4; 2 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
