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I-MAX LIGHTENING 5
I-MAX LIGHTENING 5 - 42952-201-12 - (HYDROQUINONE)
Drug Information of I-MAX LIGHTENING 5
| Product NDC: | 42952-201 |
| Proprietary Name: | I-MAX LIGHTENING 5 |
| 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 I-MAX LIGHTENING 5
| Product NDC: | 42952-201 |
| Labeler Name: | MAXLIFE USA, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120918 |
Package Information of I-MAX LIGHTENING 5
| Package NDC: | 42952-201-12 |
| Package Description: | 59 g in 1 TUBE (42952-201-12) |
NDC Information of I-MAX LIGHTENING 5
| NDC Code | 42952-201-12 |
| Proprietary Name | I-MAX LIGHTENING 5 |
| Package Description | 59 g in 1 TUBE (42952-201-12) |
| Product NDC | 42952-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120918 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MAXLIFE USA, INC. |
| Substance Name | HYDROQUINONE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
