Blistex - 10157-9831-1 - (Octinoxate, Oxybenzone, and Dimethicone)

Alphabetical Index


Drug Information of Blistex

Product NDC: 10157-9831
Proprietary Name: Blistex
Non Proprietary Name: Octinoxate, Oxybenzone, and Dimethicone
Active Ingredient(s): 2; 7.5; 2.5    g/100g; g/100g; g/100g & nbsp;   Octinoxate, Oxybenzone, and Dimethicone
Administration Route(s): TOPICAL
Dosage Form(s): STICK
Coding System: National Drug Codes(NDC)

Labeler Information of Blistex

Product NDC: 10157-9831
Labeler Name: Blistex Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130531

Package Information of Blistex

Package NDC: 10157-9831-1
Package Description: 1 CYLINDER in 1 BLISTER PACK (10157-9831-1) > 3.69 g in 1 CYLINDER

NDC Information of Blistex

NDC Code 10157-9831-1
Proprietary Name Blistex
Package Description 1 CYLINDER in 1 BLISTER PACK (10157-9831-1) > 3.69 g in 1 CYLINDER
Product NDC 10157-9831
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Oxybenzone, and Dimethicone
Dosage Form Name STICK
Route Name TOPICAL
Start Marketing Date 20130531
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Blistex Inc.
Substance Name DIMETHICONE; OCTINOXATE; OXYBENZONE
Strength Number 2; 7.5; 2.5
Strength Unit g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Blistex


General Information