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SENSAI SILK BRIGHTENING
SENSAI SILK BRIGHTENING - 64159-6394-2 - (OCTINOXATE)
Drug Information of SENSAI SILK BRIGHTENING
| Product NDC: | 64159-6394 |
| Proprietary Name: | SENSAI SILK BRIGHTENING |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 4 g/100mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SENSAI SILK BRIGHTENING
| Product NDC: | 64159-6394 |
| Labeler Name: | KANEBO COSMETICS INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080101 |
Package Information of SENSAI SILK BRIGHTENING
| Package NDC: | 64159-6394-2 |
| Package Description: | 4.6 mL in 1 JAR (64159-6394-2) |
NDC Information of SENSAI SILK BRIGHTENING
| NDC Code | 64159-6394-2 |
| Proprietary Name | SENSAI SILK BRIGHTENING |
| Package Description | 4.6 mL in 1 JAR (64159-6394-2) |
| Product NDC | 64159-6394 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KANEBO COSMETICS INC. |
| Substance Name | OCTINOXATE |
| Strength Number | 4 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
