Storage and handling
Other information • protect the product in this container from excessive heat and direct sun
Avon Sun
- Manufacturer
- Avon Products, Inc
- Effective date
- 2013-03-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 22:35:07
Label at a glance#
ProductAvon Sun Sunscreen Face
Active ingredientHOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE
Label structure8 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients
HOMOSALATE 9.5%..................
OXYBENZONE 6.0%.....................
OCTISALATE 4.75%.....................
AVOBENZONE 3.0%...................
OCTOCRYLENE 2.8%..................
OTC - PURPOSE SECTION
Purpose
.................................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.
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.
DOSAGE & ADMINISTRATION SECTION
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 SECTION
Other information
• protect the product in this container from excessive heat and direct sun
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
WATER/EAU, BUTYLOCTYL SALICYLATE, DIMETHICONE, PEG-8, STYRENE/ACRYLATES COPOLYMER, SILICA, POLYESTER-7, OLETH-3 PHOSPHATE, NEOPENTYL GLYCOL DIHEPTANOATE, TRISILOXANE, 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, POLYESTER-8, VP/EICOSENE COPOLYMER, HYDROXYETHYL UREA, BORON NITRIDE, HYDROXYETHYL ACRYLATES/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, DIMETHICONE CROSSPOLYMER, ISOHEXADECANE, PEG-8 LAURATE, HYDROGENATED LECITHIN, POLYGLYCERYL-3 DIISOSTEARATE, POLYSORBATE 60, UREA, GLYCERIN, CALCIUM CHLORIDE, CARYLIC/CAPRIC TRIGLYCERIDE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TROMETHAMINE, DISODIUM EDTA, CAPRYLYL GLYCOL, PHENOXYETHANOL, PARFUM/FRAGRANCE
OTC - QUESTIONS SECTION
Questions?
Call toll free1-800-FOR-AVON
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10096-0294-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e072-cd31-e053-dbdaa90ab51a | 8583e9cc-b123-48ae-a08f-0a02a013452b |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10096-0294-1 | Avon SunSunscreen Face | 88 mL in 1 TUBE | LOTION | 88 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10096-0294 | AVON SUN SUNSCREEN FACE (HOMOSALATE, OXYBENZONE, OCTISALATE, AVOBENZONE, OCTOCRYLENE) LOTION [AVON PRODUCTS, INC] | 2 | Legacy NDC, 1 package rows | 20130407_8583e9cc-b123-48ae-a08f-0a02a013452b.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| AVOBENZONE | ACTIVE INGREDIENT | G63QQF2NOX | 2 | |
| HOMOSALATE | ACTIVE INGREDIENT | V06SV4M95S | 2 | |
| OCTISALATE | ACTIVE INGREDIENT | 4X49Y0596W | 2 | |
| OCTOCRYLENE | ACTIVE INGREDIENT | 5A68WGF6WM | 2 | |
| OXYBENZONE | ACTIVE INGREDIENT | 95OOS7VE0Y | 2 | |
| AVOBENZONE | ACTIVE MOIETY | G63QQF2NOX | 2 | |
| HOMOSALATE | ACTIVE MOIETY | V06SV4M95S | 2 | |
| OCTISALATE | ACTIVE MOIETY | 4X49Y0596W | 2 | |
| OCTOCRYLENE | ACTIVE MOIETY | 5A68WGF6WM | 2 | |
| OXYBENZONE | ACTIVE MOIETY | 95OOS7VE0Y | 2 |
Products#
Every source-derived product name is available through these pages.
- Avon Sun Sunscreen Face
- Homosalate, Oxybenzone, Octisalate, Avobenzone, Octocrylene
- HOMOSALATE
- OXYBENZONE
- OCTISALATE
- AVOBENZONE
- OCTOCRYLENE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10096-0294 | 10096-0294-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HOMOSALATE | V06SV4M95S | ACTIB |
| OXYBENZONE | 95OOS7VE0Y | ACTIB |
| OCTISALATE | 4X49Y0596W | ACTIB |
| AVOBENZONE | G63QQF2NOX | ACTIB |
| OCTOCRYLENE | 5A68WGF6WM | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 017eb0fc-896b-44a7-998f-d494e7a844e8 | 8583e9cc-b123-48ae-a08f-0a02a013452b | 2013-03-27 | Warnings | 017eb0fc-896b-44a7-998f-d494e7a844e8 8583e9cc-b123-48ae-a08f-0a02a013452b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.