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Desert Bambu - 65643-417-06 - (Octinoxate, Avobenzone, and Octisalate)

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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

Complete Information of Desert Bambu


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