DESERT BAMBU DARK TANNING SPF 2- octinoxate and oxybenzone spray

Desert Bambu by

Drug Labeling and Warnings

Desert Bambu by is a Otc medication manufactured, distributed, or labeled by Lifetech Resources, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

INGREDIENTS AND APPEARANCE

DESERT BAMBU  DARK TANNING SPF 2
octinoxate and oxybenzone spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65643-415
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	9.49 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	9.49 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
.Alpha.-Tocopherol Acetate, D- (UNII: A7E6112E4N)
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	06/01/2008

Labeler - Lifetech Resources, LLC (622559110)

Establishment
Name	Address	ID/FEI	Business Operations
Lifetech Resources, LLC		622559110	MANUFACTURE