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Softlips Replenish
Softlips Replenish - 10742-8782-1 - (dimethicone, octinoxate, octisalate, oxybenzone)
Drug Information of Softlips Replenish
| Product NDC: | 10742-8782 |
| Proprietary Name: | Softlips Replenish |
| Non Proprietary Name: | dimethicone, octinoxate, octisalate, oxybenzone |
| Active Ingredient(s): | 20; 75; 30; 30 mg/g; mg/g; mg/g; mg/g & nbsp; dimethicone, octinoxate, octisalate, oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Softlips Replenish
| Product NDC: | 10742-8782 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100712 |
Package Information of Softlips Replenish
| Package NDC: | 10742-8782-1 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (10742-8782-1) > 2 g in 1 TUBE |
NDC Information of Softlips Replenish
| NDC Code | 10742-8782-1 |
| Proprietary Name | Softlips Replenish |
| Package Description | 1 TUBE in 1 BLISTER PACK (10742-8782-1) > 2 g in 1 TUBE |
| Product NDC | 10742-8782 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dimethicone, octinoxate, octisalate, oxybenzone |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20100712 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | DIMETHICONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 20; 75; 30; 30 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
