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Desert Bambu
Desert Bambu - 65643-417-06 - (Octinoxate, Avobenzone, and Octisalate)
Drug Information of Desert Bambu
| Product NDC: | 65643-417 |
| Proprietary Name: | Desert Bambu |
| Non Proprietary Name: | Octinoxate, Avobenzone, and Octisalate |
| Active Ingredient(s): | 19.08; 71.55; 47.7 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Avobenzone, and Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desert Bambu
| Product NDC: | 65643-417 |
| Labeler Name: | Lifetech Resources, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080501 |
Package Information of Desert Bambu
| Package NDC: | 65643-417-06 |
| Package Description: | 180 mL in 1 BOTTLE, SPRAY (65643-417-06) |
NDC Information of Desert Bambu
| NDC Code | 65643-417-06 |
| Proprietary Name | Desert Bambu |
| Package Description | 180 mL in 1 BOTTLE, SPRAY (65643-417-06) |
| Product NDC | 65643-417 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Avobenzone, and Octisalate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20080501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Lifetech Resources, LLC |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 19.08; 71.55; 47.7 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
