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Desert Bambu

Lifetech Resources, LLC

desert BAMBŪ dark tanning spray SPF 2


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DRUG FACTS

ACTIVE INGREDIENTS

Octinoxate 1%, Oxybenzone 1%

PURPOSE

Sunscreen

USE

Helps prevent sunburn. Higher SPF gives more sunburn protection.

DIRECTIONS

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

Caprylic/Capric Triglyceride, Cyclopentasiloxane, VP/Hexadecene Copolymer, Tocopheryl Acetate, Retinyl Palmitate, Tetrahexyldecyl Ascorbate, Fragrance

PRINCIPAL DISPLAY PANEL - 180 mL Bottle Label

desert
BAMBŪ ®
dark tanning
spray SPF 2

180 mL e 6 Fl. Oz.

Desert Bambu

Desert Bambu

Octinoxate and Oxybenzone SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65643-415
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 9.49 mg
OXYBENZONE OXYBENZONE 9.49 mg

Inactive Ingredients

Ingredient Name Strength
MEDIUM-CHAIN TRIGLYCERIDES
CYCLOMETHICONE 5
VITAMIN A PALMITATE
.ALPHA.-TOCOPHEROL ACETATE, D-
TETRAHEXYLDECYL ASCORBATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65643-415-08 180 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2008-06-01


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Be sure to consult your doctor before taking any medication!
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