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Desert Bambu - 65643-418-09 - (Octinoxate and Avobenzone)

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Drug Information of Desert Bambu

Product NDC: 65643-418
Proprietary Name: Desert Bambu
Non Proprietary Name: Octinoxate and Avobenzone
Active Ingredient(s): 20; 75    mg/mL; mg/mL & nbsp;   Octinoxate and Avobenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Desert Bambu

Product NDC: 65643-418
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 Information of Desert Bambu

Package NDC: 65643-418-09
Package Description: 148 mL in 1 TUBE (65643-418-09)

NDC Information of Desert Bambu

NDC Code 65643-418-09
Proprietary Name Desert Bambu
Package Description 148 mL in 1 TUBE (65643-418-09)
Product NDC 65643-418
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate and Avobenzone
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 AVOBENZONE; OCTINOXATE
Strength Number 20; 75
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Desert Bambu


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