Product NDC: | 10742-1567 |
Proprietary Name: | Softlips Peach Mango |
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): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10742-1567 |
Labeler Name: | The Mentholatum Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100201 |
Package NDC: | 10742-1567-1 |
Package Description: | 1 TUBE in 1 BLISTER PACK (10742-1567-1) > 2 g in 1 TUBE |
NDC Code | 10742-1567-1 |
Proprietary Name | Softlips Peach Mango |
Package Description | 1 TUBE in 1 BLISTER PACK (10742-1567-1) > 2 g in 1 TUBE |
Product NDC | 10742-1567 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dimethicone, Octinoxate, Octisalate, Oxybenzone |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100201 |
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 |