Product NDC: | 10157-9800 |
Proprietary Name: | Blistex |
Non Proprietary Name: | Dimethicone, Octinoxate, and Oxybenzone |
Active Ingredient(s): | 1; 7.5; 2.5 g/100g; g/100g; g/100g & nbsp; Dimethicone, Octinoxate, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10157-9800 |
Labeler Name: | Blistex Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101101 |
Package NDC: | 10157-9800-1 |
Package Description: | 4.25 g in 1 CYLINDER (10157-9800-1) |
NDC Code | 10157-9800-1 |
Proprietary Name | Blistex |
Package Description | 4.25 g in 1 CYLINDER (10157-9800-1) |
Product NDC | 10157-9800 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dimethicone, Octinoxate, and Oxybenzone |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20101101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Blistex Inc |
Substance Name | DIMETHICONE; OCTINOXATE; OXYBENZONE |
Strength Number | 1; 7.5; 2.5 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |