Product NDC: | 10157-9875 |
Proprietary Name: | Blistex |
Non Proprietary Name: | Blistex Lip Massage |
Active Ingredient(s): | 3; 7.5; 2.7; 2.5; 43.33 g/1; g/1; g/1; g/1; g/1 & nbsp; Blistex Lip Massage |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10157-9875 |
Labeler Name: | Blistex Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091215 |
Package NDC: | 10157-9875-1 |
Package Description: | 1 GEL in 1 TUBE, WITH APPLICATOR (10157-9875-1) |
NDC Code | 10157-9875-1 |
Proprietary Name | Blistex |
Package Description | 1 GEL in 1 TUBE, WITH APPLICATOR (10157-9875-1) |
Product NDC | 10157-9875 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Blistex Lip Massage |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20091215 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Blistex Inc |
Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE; PETROLATUM |
Strength Number | 3; 7.5; 2.7; 2.5; 43.33 |
Strength Unit | g/1; g/1; g/1; g/1; g/1 |
Pharmaceutical Classes |