Home
>
National Drug Code (NDC)
>
Softlips Tint
Softlips Tint - 10742-8584-2 - (Octinoxate, Octisalate)
Drug Information of Softlips Tint
| Product NDC: | 10742-8584 |
| Proprietary Name: | Softlips Tint |
| Non Proprietary Name: | Octinoxate, Octisalate |
| Active Ingredient(s): | 75; 50 mg/g; mg/g & nbsp; Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Softlips Tint
| Product NDC: | 10742-8584 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070720 |
Package Information of Softlips Tint
| Package NDC: | 10742-8584-2 |
| Package Description: | 2 g in 1 TUBE (10742-8584-2) |
NDC Information of Softlips Tint
| NDC Code | 10742-8584-2 |
| Proprietary Name | Softlips Tint |
| Package Description | 2 g in 1 TUBE (10742-8584-2) |
| Product NDC | 10742-8584 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20070720 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | OCTINOXATE; OCTISALATE |
| Strength Number | 75; 50 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
