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Softlips
Softlips - 10742-8561-2 - (octinoxate, octisalate)
Drug Information of Softlips
| Product NDC: | 10742-8561 |
| Proprietary Name: | Softlips |
| 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
| Product NDC: | 10742-8561 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080820 |
Package Information of Softlips
| Package NDC: | 10742-8561-2 |
| Package Description: | 2 g in 1 TUBE (10742-8561-2) |
NDC Information of Softlips
| NDC Code | 10742-8561-2 |
| Proprietary Name | Softlips |
| Package Description | 2 g in 1 TUBE (10742-8561-2) |
| Product NDC | 10742-8561 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20080820 |
| 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 |
