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Extralasting
Extralasting - 10096-0230-1 - (OCTINOXATE)
Drug Information of Extralasting
| Product NDC: | 10096-0230 |
| Proprietary Name: | Extralasting |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | .1125 g/1.5g & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Extralasting
| Product NDC: | 10096-0230 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101214 |
Package Information of Extralasting
| Package NDC: | 10096-0230-1 |
| Package Description: | 1.5 g in 1 CASE (10096-0230-1) |
NDC Information of Extralasting
| NDC Code | 10096-0230-1 |
| Proprietary Name | Extralasting |
| Package Description | 1.5 g in 1 CASE (10096-0230-1) |
| Product NDC | 10096-0230 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20101214 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | OCTINOXATE |
| Strength Number | .1125 |
| Strength Unit | g/1.5g |
| Pharmaceutical Classes |
