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Porcelana Day Skin Lightening
Porcelana Day Skin Lightening - 51545-110-03 - (Hydroquinone and Octinoxate)
Drug Information of Porcelana Day Skin Lightening
| Product NDC: | 51545-110 |
| Proprietary Name: | Porcelana Day Skin Lightening |
| Non Proprietary Name: | Hydroquinone and Octinoxate |
| Active Ingredient(s): | .02; .025 g/g; g/g & nbsp; Hydroquinone and Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Porcelana Day Skin Lightening
| Product NDC: | 51545-110 |
| Labeler Name: | Ultimark Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110401 |
Package Information of Porcelana Day Skin Lightening
| Package NDC: | 51545-110-03 |
| Package Description: | 1 JAR in 1 BOX (51545-110-03) > 85 g in 1 JAR |
NDC Information of Porcelana Day Skin Lightening
| NDC Code | 51545-110-03 |
| Proprietary Name | Porcelana Day Skin Lightening |
| Package Description | 1 JAR in 1 BOX (51545-110-03) > 85 g in 1 JAR |
| Product NDC | 51545-110 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydroquinone and Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ultimark Products LLC |
| Substance Name | HYDROQUINONE; OCTINOXATE |
| Strength Number | .02; .025 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
