Product NDC: | 13537-031 |
Proprietary Name: | LBEL |
Non Proprietary Name: | Octinoxate, Octisalate, and Oxybenzone |
Active Ingredient(s): | .075; .04; .04 g/mL; g/mL; g/mL & nbsp; Octinoxate, Octisalate, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13537-031 |
Labeler Name: | Ventura Corporation Ltd. (San Juan, P.R) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110829 |
Package NDC: | 13537-031-04 |
Package Description: | 1 TUBE in 1 BOX (13537-031-04) > 5 mL in 1 TUBE (13537-031-03) |
NDC Code | 13537-031-04 |
Proprietary Name | LBEL |
Package Description | 1 TUBE in 1 BOX (13537-031-04) > 5 mL in 1 TUBE (13537-031-03) |
Product NDC | 13537-031 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, and Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110829 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ventura Corporation Ltd. (San Juan, P.R) |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | .075; .04; .04 |
Strength Unit | g/mL; g/mL; g/mL |
Pharmaceutical Classes |