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Advanced Lightning
Advanced Lightning - 24623-042-22 - (OCTINOXATE and HYDROQUINONE)
Drug Information of Advanced Lightning
| Product NDC: | 24623-042 |
| Proprietary Name: | Advanced Lightning |
| Non Proprietary Name: | OCTINOXATE and HYDROQUINONE |
| Active Ingredient(s): | .02; .02 g/g; g/g & nbsp; OCTINOXATE and HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advanced Lightning
| Product NDC: | 24623-042 |
| Labeler Name: | CBI Laboratories, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050701 |
Package Information of Advanced Lightning
| Package NDC: | 24623-042-22 |
| Package Description: | 56.7 g in 1 JAR (24623-042-22) |
NDC Information of Advanced Lightning
| NDC Code | 24623-042-22 |
| Proprietary Name | Advanced Lightning |
| Package Description | 56.7 g in 1 JAR (24623-042-22) |
| Product NDC | 24623-042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and HYDROQUINONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20050701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CBI Laboratories, Inc |
| Substance Name | HYDROQUINONE; OCTINOXATE |
| Strength Number | .02; .02 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
