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LIGHTENER
LIGHTENER - 66538-201-12 - (HYDROQUINONE)
Drug Information of LIGHTENER
| Product NDC: | 66538-201 |
| Proprietary Name: | LIGHTENER |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 1.9 g/100g & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LIGHTENER
| Product NDC: | 66538-201 |
| Labeler Name: | CRC (Cosmoceutical Research Center) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111130 |
Package Information of LIGHTENER
| Package NDC: | 66538-201-12 |
| Package Description: | 50 g in 1 JAR (66538-201-12) |
NDC Information of LIGHTENER
| NDC Code | 66538-201-12 |
| Proprietary Name | LIGHTENER |
| Package Description | 50 g in 1 JAR (66538-201-12) |
| Product NDC | 66538-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111130 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CRC (Cosmoceutical Research Center) |
| Substance Name | HYDROQUINONE |
| Strength Number | 1.9 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
