ALOE SUNSCREEN- homosalate, octisalate, avobenzone, ensulizole anf octocrylene spray

Aloe Sunscreen by

Drug Labeling and Warnings

Aloe Sunscreen by is a Otc medication manufactured, distributed, or labeled by Aloe Vera of America, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients         Purpose

Avobenzone 2.7%

Ensulizole 4.0%

Homosalate 10.0%

Octisalate 5.0%

Octocrylene 2.79%          Sunscreen

PURPOSE

Uses

• helps prevent sunburn
• if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use on damaged or broken skin

WHEN USING

When using this product keep out of eyes. Rinse with water to remove. Keep away from face to avoid breathing product.

STOP USE

Stop use and ask doctor if rash occurs

KEEP OUT OF REACH OF CHILDREN

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

INSTRUCTIONS FOR USE

Directions

Shake well before use.

• hold container 4 to 6 inches from the skin and spray generously and spread evenly by hand 15 minutes before sun exposure
• do not spray directly into face. Spray on hands then apply to face.
• rapply:
•   after 80 minutes of swimming or sweating
•   immediately after towel drying
•   at least every 2 hours
• do not apply in windy conditions
• use in well-ventilated area
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
•   limit time in the sun, especially from 10 a.m. - 2 p.m.
•   wear long-sleeve shirts, pants, hats and sunglasses
• children under 6 months: Ask a doctor

INACTIVE INGREDIENT

Inactive ingredients
acrylates/C12-22 alkyl methacrylate copolymer, acrylates copolymer, aloe barbadensis leaf juice (stabilized* aloe vera gel), butyloctyl salicylate, ceteareth-25, diethylhexyl carbonate, disodium ethylene dicocamide PEG-15 disulfate, disodium EDTA, fragrance (parfum), methylisothiazolinone, neopentyl glycol diheptanoate, panthenol, pentylene glycol, phenoxyethanol, polyester-7, propanediol, styrene/acrylates copolymer, tocopheryl acetate, triethanolamine, water (aqua)

INDICATIONS & USAGE

Other information

• protect this product from excessive heat and direct sun

QUESTIONS

Questions: Call 1-888-440-2563, Monday - Friday, 9:00 a.m. to 4:00 p.m. PT.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALOE SUNSCREEN 
homosalate, octisalate, avobenzone, ensulizole anf octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11697-319
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10.0 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g  in 100 mL
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42)	ENSULIZOLE	4.0 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3.0 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2.79 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)	29.3 g  in 100 mL
WATER (UNII: 059QF0KO0R)	27.3 g  in 100 mL
PROPANEDIOL (UNII: 5965N8W85T)	3.0 g  in 100 mL
DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)	3.0 g  in 100 mL
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)	3.0 g  in 100 mL
POLYESTER-7 (UNII: 0841698D2F)	2.4 g  in 100 mL
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)	1.9 g  in 100 mL
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)	1.6 g  in 100 mL
CETEARETH-25 (UNII: 8FA93U5T67)	0.7 g  in 100 mL
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.3 g  in 100 mL
DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W)	0.3 g  in 100 mL
PENTYLENE GLYCOL (UNII: 50C1307PZG)	0.1 g  in 100 mL
PANTHENOL (UNII: WV9CM0O67Z)	0.1 g  in 100 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.01 g  in 100 mL
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)	0.01 g  in 100 mL
EDETATE DISODIUM (UNII: 7FLD91C86K)	0.1 g  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.3 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11697-319-07	178.000 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	08/16/2010

Labeler - Aloe Vera of America, Inc. (049049463)

Registrant - Aloe Vera of America, Inc. (049049463)

Establishment
Name	Address	ID/FEI	Business Operations
Aloe Vera of America, Inc.		049049463	manufacture(11697-319)