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Softlips Lip Relief
Softlips Lip Relief - 10742-8932-1 - (skin protectant/topical analgesic)
Drug Information of Softlips Lip Relief
| Product NDC: | 10742-8932 |
| Proprietary Name: | Softlips Lip Relief |
| Non Proprietary Name: | skin protectant/topical analgesic |
| Active Ingredient(s): | 10; 5 mg/g; mg/g & nbsp; skin protectant/topical analgesic |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Softlips Lip Relief
| Product NDC: | 10742-8932 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100101 |
Package Information of Softlips Lip Relief
| Package NDC: | 10742-8932-1 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (10742-8932-1) > 8 g in 1 TUBE |
NDC Information of Softlips Lip Relief
| NDC Code | 10742-8932-1 |
| Proprietary Name | Softlips Lip Relief |
| Package Description | 1 TUBE in 1 BLISTER PACK (10742-8932-1) > 8 g in 1 TUBE |
| Product NDC | 10742-8932 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | skin protectant/topical analgesic |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | ALLANTOIN; MENTHOL |
| Strength Number | 10; 5 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
