DESERT BAMBU SUNSCREEN SPF 15- octinoxate and avobenzone lotion

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 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.

INGREDIENTS AND APPEARANCE

DESERT BAMBU  SUNSCREEN SPF 15
octinoxate and avobenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65643-418
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75.00 mg  in 1 mL
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	20.00 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2)
Stearic Acid (UNII: 4ELV7Z65AP)
Polyoxyl 100 Stearate (UNII: YD01N1999R)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Ethylhexyl Palmitate (UNII: 2865993309)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Dimethicone (UNII: 92RU3N3Y1O)
Shea Butter (UNII: K49155WL9Y)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Squalane (UNII: GW89575KF9)
Green Tea Leaf (UNII: W2ZU1RY8B0)
.Alpha.-Tocopherol Acetate, D- (UNII: A7E6112E4N)
Hyaluronate Sodium (UNII: YSE9PPT4TH)
Ascorbyl Palmitate (UNII: QN83US2B0N)
Vitamin A Palmitate (UNII: 1D1K0N0VVC)
Steareth-2 (UNII: V56DFE46J5)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Butylene Glycol (UNII: 3XUS85K0RA)
Trolamine (UNII: 9O3K93S3TK)
Imidurea (UNII: M629807ATL)
Edetate Disodium (UNII: 7FLD91C86K)
Methylparaben (UNII: A2I8C7HI9T)
Propylparaben (UNII: Z8IX2SC1OH)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65643-418-09	148 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/01/2008

Labeler - Lifetech Resources, LLC (622559110)

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