| 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 |