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Softlips Replenish - 10742-8782-9 - (dimethicone, octinoxate, octisalate, oxybenzone)

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Drug Information of Softlips Replenish

Product NDC: 10742-8782
Proprietary Name: Softlips Replenish
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)

Labeler Information of Softlips Replenish

Product NDC: 10742-8782
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100712

Package Information of Softlips Replenish

Package NDC: 10742-8782-9
Package Description: 2 TUBE in 1 BLISTER PACK (10742-8782-9) > 2 g in 1 TUBE

NDC Information of Softlips Replenish

NDC Code 10742-8782-9
Proprietary Name Softlips Replenish
Package Description 2 TUBE in 1 BLISTER PACK (10742-8782-9) > 2 g in 1 TUBE
Product NDC 10742-8782
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dimethicone, octinoxate, octisalate, oxybenzone
Dosage Form Name STICK
Route Name TOPICAL
Start Marketing Date 20100712
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 Replenish


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