Home
>
National Drug Code (NDC)
>
Softlips Pure
Softlips Pure - 10742-6761-1 - (Zinc oxide)
Drug Information of Softlips Pure
| Product NDC: | 10742-6761 |
| Proprietary Name: | Softlips Pure |
| Non Proprietary Name: | Zinc oxide |
| Active Ingredient(s): | 55 mg/g & nbsp; Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Softlips Pure
| Product NDC: | 10742-6761 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
Package Information of Softlips Pure
| Package NDC: | 10742-6761-1 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (10742-6761-1) > 10 g in 1 TUBE |
NDC Information of Softlips Pure
| NDC Code | 10742-6761-1 |
| Proprietary Name | Softlips Pure |
| Package Description | 1 TUBE in 1 BLISTER PACK (10742-6761-1) > 10 g in 1 TUBE |
| Product NDC | 10742-6761 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc oxide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | ZINC OXIDE |
| Strength Number | 55 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
