Product NDC: | 13537-148 |
Proprietary Name: | LBel |
Non Proprietary Name: | TITANIUM DIOXIDE, OXYBENZONE, and OCTINOXATE |
Active Ingredient(s): | .04; .03; .04425 g/g; g/g; g/g & nbsp; TITANIUM DIOXIDE, OXYBENZONE, and OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-148 |
Labeler Name: | Ventura Corporation Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120124 |
Package NDC: | 13537-148-04 |
Package Description: | 1 CASE in 1 BOX (13537-148-04) > 7.8 g in 1 CASE (13537-148-03) |
NDC Code | 13537-148-04 |
Proprietary Name | LBel |
Package Description | 1 CASE in 1 BOX (13537-148-04) > 7.8 g in 1 CASE (13537-148-03) |
Product NDC | 13537-148 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TITANIUM DIOXIDE, OXYBENZONE, and OCTINOXATE |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20120124 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura Corporation Ltd |
Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | .04; .03; .04425 |
Strength Unit | g/g; g/g; g/g |
Pharmaceutical Classes |