Product NDC: | 10742-8596 |
Proprietary Name: | Softlips Flavor Fusions Strawberry Banana |
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) |
Product NDC: | 10742-8596 |
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: | 10742-8596-3 |
Package Description: | 2 g in 1 TUBE (10742-8596-3) |
NDC Code | 10742-8596-3 |
Proprietary Name | Softlips Flavor Fusions Strawberry Banana |
Package Description | 2 g in 1 TUBE (10742-8596-3) |
Product NDC | 10742-8596 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dimethicone, octinoxate, octisalate, 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; OCTISALATE; OXYBENZONE |
Strength Number | 20; 75; 30; 30 |
Strength Unit | mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |