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Maybelline New York Instant Age Rewind Eraser
Maybelline New York Instant Age Rewind Eraser - 49967-006-01 - (Octinoxate)
Drug Information of Maybelline New York Instant Age Rewind Eraser
| Product NDC: | 49967-006 |
| Proprietary Name: | Maybelline New York Instant Age Rewind Eraser |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 1.5 mL/20mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Maybelline New York Instant Age Rewind Eraser
| Product NDC: | 49967-006 |
| Labeler Name: | L'Oreal USA Products Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091001 |
Package Information of Maybelline New York Instant Age Rewind Eraser
| Package NDC: | 49967-006-01 |
| Package Description: | 20 mL in 1 BOTTLE, WITH APPLICATOR (49967-006-01) |
NDC Information of Maybelline New York Instant Age Rewind Eraser
| NDC Code | 49967-006-01 |
| Proprietary Name | Maybelline New York Instant Age Rewind Eraser |
| Package Description | 20 mL in 1 BOTTLE, WITH APPLICATOR (49967-006-01) |
| Product NDC | 49967-006 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | OCTINOXATE |
| Strength Number | 1.5 |
| Strength Unit | mL/20mL |
| Pharmaceutical Classes |
