DESERT BAMBU- octinoxate, octocrylene, octisalate, and zinc oxide cream

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%, Octocrylene 6.0%, Octisalate 5.0%, Zinc Oxide 2.94%

PURPOSE

Sunscreen

USE

Helps prevent sunburn. Higher SPF gives more sunburn protection.

DIRECTIONS FOR USE

Apply evenly and liberally to all exposed facial 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, Ethylhexyl Isononanoate, Acrylates Copolymer, Butylene Glycol, PEG-100 Stearate, Cetyl Alcohol, Glyceryl Stearate, Sorbitan Stearate, Polysorbate 60, Dimethicone, Squalane, Hydroxylated Lecithin, Allantoin, Tocopheryl Acetate, Centella Asiatica Extract, Echinacea Angustifolia Extract, Vitis Vinifera (Grape) Seed Extract, Citrus Medica Limonum (Lemon) Peel Extract, Melissa Officinalis Extract, Triethoxycaprylylsilane, Xanthan Gum, Disodium EDTA, Imidazolidinyl Urea, Methylparaben, Propylparaben

PRINCIPAL DISPLAY PANEL- 118 mL Tube Label

desert
BAMBŪ®
facial sunscreen
SPF 30

118 mL e 4 Fl. Oz.

INGREDIENTS AND APPEARANCE

DESERT BAMBU   FACIAL SUNSCREEN SPF 30
octinoxate, octocrylene, octisalate, and zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65643-165
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	74.025 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	59.22 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	49.35 mg  in 1 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	2.902 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Polyoxyl 100 Stearate (UNII: YD01N1999R)
Sorbitan Monostearate (UNII: NVZ4I0H58X)
Polysorbate 60 (UNII: CAL22UVI4M)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Butylene Glycol (UNII: 3XUS85K0RA)
Cetyl Alcohol (UNII: 936JST6JCN)
Dimethicone (UNII: 92RU3N3Y1O)
Squalane (UNII: GW89575KF9)
Allantoin (UNII: 344S277G0Z)
.Alpha.-Tocopherol Acetate, D- (UNII: A7E6112E4N)
Centella Asiatica (UNII: 7M867G6T1U)
Echinacea Angustifolia (UNII: VB06AV5US8)
Lemon Peel (UNII: 72O054U628)
Melissa Officinalis (UNII: YF70189L0N)
Xanthan Gum (UNII: TTV12P4NEE)
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: 65643-165-04	118 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	03/01/2008

Labeler - Lifetech Resources, LLC (622559110)

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