Softlips - 10742-8561-2 - (octinoxate, octisalate)

Alphabetical Index


Drug Information of Softlips

Product NDC: 10742-8561
Proprietary Name: Softlips
Non Proprietary Name: octinoxate, octisalate
Active Ingredient(s): 75; 50    mg/g; mg/g & nbsp;   octinoxate, octisalate
Administration Route(s): TOPICAL
Dosage Form(s): LIPSTICK
Coding System: National Drug Codes(NDC)

Labeler Information of Softlips

Product NDC: 10742-8561
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080820

Package Information of Softlips

Package NDC: 10742-8561-2
Package Description: 2 g in 1 TUBE (10742-8561-2)

NDC Information of Softlips

NDC Code 10742-8561-2
Proprietary Name Softlips
Package Description 2 g in 1 TUBE (10742-8561-2)
Product NDC 10742-8561
Product Type Name HUMAN OTC DRUG
Non Proprietary Name octinoxate, octisalate
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20080820
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Mentholatum Company
Substance Name OCTINOXATE; OCTISALATE
Strength Number 75; 50
Strength Unit mg/g; mg/g
Pharmaceutical Classes

Complete Information of Softlips


General Information