AVON SUN SUNSCREEN- homosalate, octinoxate, octisalate, oxybenzone, avobenzone, octocrylene aerosol, spray

Avon Sun by

Drug Labeling and Warnings

Avon Sun by is a Otc medication manufactured, distributed, or labeled by New Avon LLC, Accra Pac, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients
HOMOSALATE 8.00%..................

OCTINOXATE 7.5%.....................

OCTISALATE 4.75%.....................

OXYBENZONE 4.75%.....................

AVOBENZONE 2.85%...................

OCTOCRYLENE 2.56%..................

Purpose
.................................Sunscreen

.................................Sunscreen

.................................Sunscreen

.................................Sunscreen

.................................Sunscreen

.................................Sunscreen

INDICATIONS & USAGE

Uses
helps prevent sunburn

WARNINGS

Warnings
For external use only

Do not use on damaged or broken skin

When using this product

• keep out of eyes. Rinse with water to remove.
• keep away from face to avoid breathing it.

Stop use and ask a doctor if rash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

​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 temparatures above 120F (50C). Do not tamper with valve closure or puncture or incinerate can.

DOSAGE & ADMINISTRATION

Directions
spray generously and spread evenly by hand 15 minutes before sun exposure

hold container 4 to 6 inches from skin to apply

do not spray directly into face

Spray on hands, then apply to face

do not apply in windy conditions

use in well-ventilated areas
children under 6 months of age: ask a doctor

Reapply after 80 minutes of swimming or sweating

  immediately after towel drying

  at least every 2 hours

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 value 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-sleeved shirts, pants, hats, and sunglasses

STORAGE AND HANDLING

Other information

protect the product in this container from excessive heat and direct sun

INACTIVE INGREDIENT

Inactive Ingredients:
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

QUESTIONS

Questions?
Call toll free1-800-FOR-AVON

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AVON SUN  SUNSCREEN
homosalate, octinoxate, octisalate, oxybenzone, avobenzone, octocrylene aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0296
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	80 mg  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	75 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	47.5 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	47.5 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	28.5 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	25.6 mg  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0296-1	136.5 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	03/26/2013

Labeler - New Avon LLC (080143520)

Establishment
Name	Address	ID/FEI	Business Operations
Accra Pac, Inc.		024213616	manufacture(10096-0296)