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NeoStrata HQ Skin Lightening
NeoStrata HQ Skin Lightening - 58414-8808-1 - (HYDROQUINONE)
Drug Information of NeoStrata HQ Skin Lightening
| Product NDC: | 58414-8808 |
| Proprietary Name: | NeoStrata HQ Skin Lightening |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | .02 g/g & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NeoStrata HQ Skin Lightening
| Product NDC: | 58414-8808 |
| Labeler Name: | NeoStrata Company Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110222 |
Package Information of NeoStrata HQ Skin Lightening
| Package NDC: | 58414-8808-1 |
| Package Description: | 1 TUBE in 1 CARTON (58414-8808-1) > 30 g in 1 TUBE |
NDC Information of NeoStrata HQ Skin Lightening
| NDC Code | 58414-8808-1 |
| Proprietary Name | NeoStrata HQ Skin Lightening |
| Package Description | 1 TUBE in 1 CARTON (58414-8808-1) > 30 g in 1 TUBE |
| Product NDC | 58414-8808 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110222 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NeoStrata Company Inc |
| Substance Name | HYDROQUINONE |
| Strength Number | .02 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
