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Scarlight MD
Scarlight MD - 64269-9902-7 - (HYDROQUINONE)
Drug Information of Scarlight MD
| Product NDC: | 64269-9902 |
| Proprietary Name: | Scarlight MD |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 20 mg/mL & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Scarlight MD
| Product NDC: | 64269-9902 |
| Labeler Name: | Scarguard Labs, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20021101 |
Package Information of Scarlight MD
| Package NDC: | 64269-9902-7 |
| Package Description: | 15 mL in 1 BOTTLE, WITH APPLICATOR (64269-9902-7) |
NDC Information of Scarlight MD
| NDC Code | 64269-9902-7 |
| Proprietary Name | Scarlight MD |
| Package Description | 15 mL in 1 BOTTLE, WITH APPLICATOR (64269-9902-7) |
| Product NDC | 64269-9902 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20021101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Scarguard Labs, LLC |
| Substance Name | HYDROQUINONE |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
