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HYPERPIGMENTATION TREATMENT
HYPERPIGMENTATION TREATMENT - 46007-301-12 - (HYDROQUINONE)
Drug Information of HYPERPIGMENTATION TREATMENT
| Product NDC: | 46007-301 |
| Proprietary Name: | HYPERPIGMENTATION TREATMENT |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 2 g/100mL & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYPERPIGMENTATION TREATMENT
| Product NDC: | 46007-301 |
| Labeler Name: | Skin Authority LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120419 |
Package Information of HYPERPIGMENTATION TREATMENT
| Package NDC: | 46007-301-12 |
| Package Description: | 50 mL in 1 BOTTLE (46007-301-12) |
NDC Information of HYPERPIGMENTATION TREATMENT
| NDC Code | 46007-301-12 |
| Proprietary Name | HYPERPIGMENTATION TREATMENT |
| Package Description | 50 mL in 1 BOTTLE (46007-301-12) |
| Product NDC | 46007-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120419 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Skin Authority LLC |
| Substance Name | HYDROQUINONE |
| Strength Number | 2 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
