Avon Sun

Manufacturer
New Avon LLC | Accra Pac, Inc.
Effective date
2016-02-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:45:17

Label at a glance#

ProductAvon Sun Sunscreen
Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE
Label structure8 sections

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

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

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

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

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

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

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

OTC - PURPOSE SECTION

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

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

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

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

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

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

INDICATIONS & USAGE SECTION

Uses
• helps prevent sunburn

WARNINGS SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

When using this product

  • keep out of eyes. Rinse with water to remove.
  • keep away from face to avoid breathing it.
OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

GENERAL PRECAUTIONS SECTION

​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 SECTION

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 SECTION

Other information

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

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions?
Call toll free1-800-FOR-AVON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0296-12020-01-31C16284748780-19d75b9cf-daed-f424-e053-dadaa90a57ce9d7238bb-8237-4cc8-8c4d-8d815a22a166

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0296-1Avon SunSunscreen136.5 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY136.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0296AVON SUN SUNSCREEN (HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE) AEROSOL, SPRAY [NEW AVON LLC]2Legacy NDC, 1 package rows20160303_9d7238bb-8237-4cc8-8c4d-8d815a22a166.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
HOMOSALATEACTIVE INGREDIENTV06SV4M95S1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM1
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
HOMOSALATEACTIVE MOIETYV06SV4M95S1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1
OXYBENZONEACTIVE MOIETY95OOS7VE0Y1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-029610096-0296-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
340b9d54-984a-46d1-ba40-1ad4fc5c63939d7238bb-8237-4cc8-8c4d-8d815a22a1662016-02-17WarningsExact identifier
spl id: 340b9d54-984a-46d1-ba40-1ad4fc5c6393
spl set id: 9d7238bb-8237-4cc8-8c4d-8d815a22a166

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.