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Ultra Color Rich
Ultra Color Rich - 10096-0191-1 - (OCTINOXATE)
Drug Information of Ultra Color Rich
| Product NDC: | 10096-0191 |
| Proprietary Name: | Ultra Color Rich |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 210 mg/3g & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra Color Rich
| Product NDC: | 10096-0191 |
| Labeler Name: | Avon Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091229 |
Package Information of Ultra Color Rich
| Package NDC: | 10096-0191-1 |
| Package Description: | 3 g in 1 CASE (10096-0191-1) |
NDC Information of Ultra Color Rich
| NDC Code | 10096-0191-1 |
| Proprietary Name | Ultra Color Rich |
| Package Description | 3 g in 1 CASE (10096-0191-1) |
| Product NDC | 10096-0191 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20091229 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Avon Products, Inc. |
| Substance Name | OCTINOXATE |
| Strength Number | 210 |
| Strength Unit | mg/3g |
| Pharmaceutical Classes |
