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Softlips Tint - 10742-8584-9 - (Octinoxate, Octisalate)

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Drug Information of Softlips Tint

Product NDC: 10742-8584
Proprietary Name: Softlips Tint
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 Tint

Product NDC: 10742-8584
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070720

Package Information of Softlips Tint

Package NDC: 10742-8584-9
Package Description: 2 TUBE in 1 BLISTER PACK (10742-8584-9) > 2 g in 1 TUBE

NDC Information of Softlips Tint

NDC Code 10742-8584-9
Proprietary Name Softlips Tint
Package Description 2 TUBE in 1 BLISTER PACK (10742-8584-9) > 2 g in 1 TUBE
Product NDC 10742-8584
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octisalate
Dosage Form Name LIPSTICK
Route Name TOPICAL
Start Marketing Date 20070720
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 Tint


General Information