Softlips - 10742-8470-9 - (dimethicone, octinoxate, octisalate, oxybenzone)

Alphabetical Index


Drug Information of Softlips

Product NDC: 10742-8470
Proprietary Name: Softlips
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)

Labeler Information of Softlips

Product NDC: 10742-8470
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070112

Package Information of Softlips

Package NDC: 10742-8470-9
Package Description: 2 TUBE in 1 BLISTER PACK (10742-8470-9) > 2 g in 1 TUBE

NDC Information of Softlips

NDC Code 10742-8470-9
Proprietary Name Softlips
Package Description 2 TUBE in 1 BLISTER PACK (10742-8470-9) > 2 g in 1 TUBE
Product NDC 10742-8470
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dimethicone, octinoxate, octisalate, oxybenzone
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20070112
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

Complete Information of Softlips


General Information