Product NDC: | 65643-419 |
Proprietary Name: | Desert Bambu |
Non Proprietary Name: | Octinoxate, Octocrylene, Oxybenzone, and Titanium Dioxide |
Active Ingredient(s): | 73.5; 68.25; 57.75; 47.25 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octocrylene, Oxybenzone, and Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65643-419 |
Labeler Name: | Lifetech Resources, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080401 |
Package NDC: | 65643-419-10 |
Package Description: | 148 mL in 1 TUBE (65643-419-10) |
NDC Code | 65643-419-10 |
Proprietary Name | Desert Bambu |
Package Description | 148 mL in 1 TUBE (65643-419-10) |
Product NDC | 65643-419 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octocrylene, Oxybenzone, and Titanium Dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20080401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Lifetech Resources, LLC |
Substance Name | OCTINOXATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 73.5; 68.25; 57.75; 47.25 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |