Solutions

Manufacturer
Avon Products, Inc
Effective date
2013-02-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:34:32

Label at a glance#

ProductSolutions A.M. Total Radiance
Active ingredientOCTINOXATE, OCTISALATE, AVOBENZONE
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
Octinoxate 7.5%.......................................
Octisalate 5.0%........................................
Avobenzone 2.0%....................................

OTC - PURPOSE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Uses
• helps prevent sunburn

WARNINGS SECTION

Warnings
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
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 at least every 2 hours
• use a water resistant sunscreen if swimming or sweating

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients
Water, Butylene Glycol, Glycerin, Cyclopentasiloxane, Hydrogenated Polyisobutene, Hydroxyethyl Urea, Dimethicone, Lauryl Lactate, Dilauryl Thiodipropionate, Calcium PCA, Lactoferrin, Palmitoyl Oligopeptide, Saccharomyces Ferment Filtrate, Saccharomyces Lysate Extract, Phospholipids, Phytol, Tocopheryl Acetate, Aframomum Melegueta Seed Extract, Butyrospermum Parkii (Shea Butter), Ceramide 2, Cholesterol, DNA, Foeniculum Vulgare (Fennel) Seed Extract, Viola Tricolor Extract, Yeast Extract, PEG-10 Rapeseed Sterol, Urea, Caprylic/Capric Triglyceride, C12-15 Alkyl Benzoate, PEG-100 Stearate, Pentylene Glycol, Hexylene Glycol, Caprylyl Glycol, Boron Nitride, Silica, Isohexadecane, Cetyl Alcohol, Dimethiconol, Tribehenin, Polysorbate 60, Sorbitan Isostearate, Xanthan Gum, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Butylene/Ethylene/Styrene Copolymer, Ethylene/Propylene/Styrene Copolymer, Dimethicone Crosspolymer, Fragrance, Carbomer, Sodium Dehydroacetate, Chlorphenesin, Disodium EDTA, Phenoxyethanol, Sodium Hydroxide.

OTC - QUESTIONS SECTION

Questions or comments?
Call toll free 1-800-FOR-AVON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of cartonimage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0168-22019-11-27C16284748780-19855d018-d9e8-cd31-e053-dbdaa90ab51a3fcd712a-b6d1-4ff3-8c97-3abe3d9ca73f
10096-0168-32019-11-27C16284748780-19855d018-d9e8-cd31-e053-dbdaa90ab51a3fcd712a-b6d1-4ff3-8c97-3abe3d9ca73f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0168-1SolutionsA.M. Total Radiance118 mL in 1 BOTTLE, PUMPLOTION1181
10096-0168-2SolutionsA.M. Total Radiance1 in 1 CARTONLOTION11
10096-0168-3SolutionsA.M. Total Radiance1.1 mL in 1 PACKAGELOTION1.11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0168SOLUTIONS A.M. TOTAL RADIANCE (OCTINOXATE, OCTISALATE, AVOBENZONE) LOTION [AVON PRODUCTS, INC]1Legacy NDC, 3 package rows20130214_3fcd712a-b6d1-4ff3-8c97-3abe3d9ca73f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-016810096-0168-1, 10096-0168-2, 10096-0168-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB

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
084a9c9c-d070-4b8a-a5af-cde88b052bf13fcd712a-b6d1-4ff3-8c97-3abe3d9ca73f2013-02-08WarningsExact identifier
spl id: 084a9c9c-d070-4b8a-a5af-cde88b052bf1
spl set id: 3fcd712a-b6d1-4ff3-8c97-3abe3d9ca73f

Reported adverse events (FAERS/openFDA)#

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