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Skin Lightening
Skin Lightening - 14222-1615-2 - (HYDROQUINONE)
Drug Information of Skin Lightening
| Product NDC: | 14222-1615 |
| Proprietary Name: | Skin Lightening |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 2 mL/100mL & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Skin Lightening
| Product NDC: | 14222-1615 |
| Labeler Name: | Rodan & Fields, LLC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110606 |
Package Information of Skin Lightening
| Package NDC: | 14222-1615-2 |
| Package Description: | 1 TUBE in 1 BOX (14222-1615-2) > 125 mL in 1 TUBE (14222-1615-1) |
NDC Information of Skin Lightening
| NDC Code | 14222-1615-2 |
| Proprietary Name | Skin Lightening |
| Package Description | 1 TUBE in 1 BOX (14222-1615-2) > 125 mL in 1 TUBE (14222-1615-1) |
| Product NDC | 14222-1615 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rodan & Fields, LLC. |
| Substance Name | HYDROQUINONE |
| Strength Number | 2 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
