ANEW SOLAR ADVANCE SUNSCREEN BODY MIST- homosalate, octinoxate, octisalate, oxybenzone, avobenzone, octocrylene spray

ANEW Solar Advance by

Drug Labeling and Warnings

ANEW Solar Advance by is a Otc medication manufactured, distributed, or labeled by Avon Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

To Use: Apply liberally and evenly 15 minutes before sun
exposure. Spray evenly over skin and rub in. Reapply as
needed or after towel drying, swimming, or perspiring. Children
under 6 months of age: ask a doctor.

WARNINGS

Warning: For external use only. When using this product, keep
out of eyes. Rinse thoroughly with water to remove. Stop use
and ask a doctor if rash or irritation develops and lasts. Keep
out of reach of children.

INDICATIONS & USAGE

Uses: Helps prevent sunburn. Higher SPF gives more
sunscreen protection. Moderate sun protection product.
Retains SPF after 80 minutes of activity in the water.

SAFE HANDLING WARNING

Flammable, contents under pressure. Keep away from flame,
fire or extreme heat. Do not place in hot water or near
radiators, stove, or other sources of heat. Do not use in
presence of open flame or sparks. Do not store at
temperatures above 120°F.

ACTIVE INGREDIENT

ACTIVE INGREDIENTS/ INGREDIENTES ACTIVOS:
HOMOSALATE 8.00%, OCTINOXATE 7.5%, OCTISALATE
4.75%, OXYBENZONE 4.75%, AVOBENZONE 2.85%,
OCTOCRYLENE 2.56%.

INACTIVE INGREDIENT

OTHER INGREDIENTS/OTROS INGREDIENTES: SD
ALCOHOL 40-B, C12-15 ALKYL BENZOATE, PPG-2
MYRISTYL ETHER PROPIONATE, DIMETHICONE, GLYCERIN,
ACRYLATES/OCTYLACRYLAMIDE COPOLYMER,
POLYESTER-8, DILAURYL THIODIPROPIONATE,
KAEMPFERIA GALANGA ROOT EXTRACT, GLYCINE SOJA
(SOYBEAN) SEED EXTRACT, PHAEODACTYLUM
TRICORNUTUM EXTRACT, ORYZANOL, FOENICULUM
VULGARE (FENNEL) FRUIT EXTRACT, DAUCUS CAROTA
SATIVA (CARROT) ROOT EXTRACT, TOCOPHEROL,
CAPRYLIC/CAPRIC TRIGLYCERIDE, CAPRYLYL GLYCOL,
PARFUM/ FRAGRANCE, WATER/EAU.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANEW SOLAR ADVANCE  SUNSCREEN BODY MIST
homosalate, octinoxate, octisalate, oxybenzone, avobenzone, octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0254
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	12 mL  in 150 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	11.25 mL  in 150 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	7.125 mL  in 150 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	7.125 mL  in 150 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	4.275 mL  in 150 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3.84 mL  in 150 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0254-2	1 in 1 CARTON
1	NDC: 10096-0254-1	150 mL in 1 CAN

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	04/11/2011

Labeler - Avon Products, Inc. (001468693)