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SKIN LIGHTENING COMPLEX
SKIN LIGHTENING COMPLEX - 65113-8401-1 - (HYDROQUINONE)
Drug Information of SKIN LIGHTENING COMPLEX
| Product NDC: | 65113-8401 |
| Proprietary Name: | SKIN LIGHTENING COMPLEX |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 2 g/100g & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SKIN LIGHTENING COMPLEX
| Product NDC: | 65113-8401 |
| Labeler Name: | G.S. COSMECEUTICAL USA, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091209 |
Package Information of SKIN LIGHTENING COMPLEX
| Package NDC: | 65113-8401-1 |
| Package Description: | 30 g in 1 TUBE (65113-8401-1) |
NDC Information of SKIN LIGHTENING COMPLEX
| NDC Code | 65113-8401-1 |
| Proprietary Name | SKIN LIGHTENING COMPLEX |
| Package Description | 30 g in 1 TUBE (65113-8401-1) |
| Product NDC | 65113-8401 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20091209 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | G.S. COSMECEUTICAL USA, INC. |
| Substance Name | HYDROQUINONE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
