AVON SUN SUNSCREEN- homosalate, oxybenzone, octisalate, avobenzone, octocrylene lotion

Avon Sun by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

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

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

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

AVOBENZONE 2.80%...................

OCTOCRYLENE 2.50%..................

Purpose
.................................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.

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.

DOSAGE & ADMINISTRATION

Directions
apply generously and evenly 15 minutes before sun exposure
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:
WATER/EAU, BUTYLOCTYL SALICYLATE, BUTYLENE GLYCOL, GLYCERIN, PEG-8, POLYESTER-7, NEOPENTYL GLYCOL DIHEPTANOATE, VP/EICOSENE COPOLYMER, DIMETHICONE, CAPRYLYL GLYCOL, CETYL ALCOHOL, TROMETHAMINE, GLYCERYL STEARATE, TRIMETHYLSILOXYSILICATE, HYDROGENATED LECITHIN, CARBOMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, DISODIUM EDTA,
POLYGLYCERYL-3 DIISOSTEARATE, 1,2-HEXANEDIOL, METHYLBENZYL ALCOHOL, PARFUM/FRAGRANCE, ALOE BARBADENSIS LEAF EXTRACT, PANTHENOL, TOCOPHERYL ACETATE, PHYTOL, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT,

QUESTIONS

Questions?
Call toll free1-800-FOR-AVON

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AVON SUN  SUNSCREEN
homosalate, oxybenzone, octisalate, avobenzone, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10096-0295
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 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	47.5 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	47.5 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	28 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	25 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10096-0295-1	236 mL in 1 TUBE; 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
Avon Products, Inc		005149471	manufacture(10096-0295)