Product NDC: | 10742-8456 |
Proprietary Name: | Softlips Intense Moisture Double Mint |
Non Proprietary Name: | dimethicone, octinoxate, oxybenzone |
Active Ingredient(s): | 20; 75; 30 mg/g; mg/g; mg/g & nbsp; dimethicone, octinoxate, oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10742-8456 |
Labeler Name: | The Mentholatum Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130601 |
Package NDC: | 10742-8456-2 |
Package Description: | 2 TUBE in 1 BLISTER PACK (10742-8456-2) > 2 g in 1 TUBE |
NDC Code | 10742-8456-2 |
Proprietary Name | Softlips Intense Moisture Double Mint |
Package Description | 2 TUBE in 1 BLISTER PACK (10742-8456-2) > 2 g in 1 TUBE |
Product NDC | 10742-8456 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dimethicone, octinoxate, oxybenzone |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20130601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | The Mentholatum Company |
Substance Name | DIMETHICONE; OCTINOXATE; OXYBENZONE |
Strength Number | 20; 75; 30 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |