Desert Bambu Sunscreen SPF 15

Dosage form: lotion
Ingredients: Octinoxate 75.00mg in 1mL, Avobenzone 20.00mg in 1mL
Labeler: Lifetech Resources, LLC
NDC Code: 65643-418

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

desert
BAMBŪ®
sunscreen lotion
SPF 15

DRUG FACTS

ACTIVE INGREDIENTS

Octinoxate 7.5%, Avobenzone 2.0%

PURPOSE

Sunscreen

USE

Helps prevent sunburn. Higher SPF gives more sunburn protection.

DIRECTIONS FOR USE

Apply evenly and liberally to all exposed areas before sun exposure. Ensure complete coverage. Reapply as needed or after swimming, towel drying, perspiring, or vigorous activity. Ask a doctor before use on children under 6 months of age.

WARNINGS

For external use only.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENTS

Water, Cyclopentasiloxane, Acrylates Copolymer, Ethylhexyl Isononanoate, Sodium PCA, Stearic Acid PEG-100 Stearate, Aloe Barbadensis Leaf Juice, Ethylhexyl Palmitate, Glyceryl Stearate, Dimethicone, Butyrospermum Parkii (Shea Butter), Magnesium Aluminum Silicate, Squalane, Pinus Taeda Bark Extract, Camellia Sinensis Leaf Extract, Vitis Vinifera (Grape) Seed Extract, Lecithin, Tocopheryl Acetate, Ascorbyl Palmitate, Retinyl Palmitate, Sodium Hyaluronate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Steareth-2, Cetearyl Alcohol Butylene Glycol, Triethanolamine, Disodium EDTA, Methylparaben, Propylparaben, Imidazolidinyl Urea

PRINCIPAL DISPLAY PANEL - 148 mL Tube Label

desert
BAMBŪ®
sunscreen lotion
SPF 15

148 mL e 5 Fl. Oz.

DESERT BAMBU  SUNSCREEN SPF 15
octinoxate and avobenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65643-418
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (Octinoxate) Octinoxate75.00 mg  in 1 mL
Avobenzone (Avobenzone) Avobenzone20.00 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Cyclomethicone 5 
Sodium Pyrrolidone Carboxylate 
Stearic Acid 
Polyoxyl 100 Stearate 
Aloe Vera Leaf 
Ethylhexyl Palmitate 
Glyceryl Monostearate 
Dimethicone 
Shea Butter 
Magnesium Aluminum Silicate 
Squalane 
Green Tea Leaf 
.Alpha.-Tocopherol Acetate, D- 
Hyaluronate Sodium 
Ascorbyl Palmitate 
Vitamin A Palmitate 
Steareth-2 
Cetostearyl Alcohol 
Butylene Glycol 
Trolamine 
Imidurea 
Edetate Disodium 
Methylparaben 
Propylparaben 
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:65643-418-09148 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35204/01/2008
Labeler - Lifetech Resources, LLC (622559110)
Establishment
NameAddressID/FEIOperations
Lifetech Resources, LLC622559110MANUFACTURE

Revised: 09/2010
 
Lifetech Resources, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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