Solutions

Manufacturer: Avon Products, Inc
Effective date: 2013-01-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:34:37

Label at a glance#

ProductSolutions Ageless Results Day

Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE

Label structure8 sections

Storage and handling

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

Contacts and useful links#

PhoneLabel contact1-800-FOR-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
OCTINOXATE 7.5%.........................................................
OCTISALATE 5.0%.........................................................
OXYBENZONE 4.0%.........................................................
AVOBENZONE 2.0%.......................................................

OTC - PURPOSE SECTION

Purpose

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

INDICATIONS & USAGE 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 liberally 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/EAU, CYCLOPENTASILOXANE, GLYCERIN, BUTYLENE GLYCOL, C12-15 ALKYL BENZOATE, COFFEA ARABICA
(COFFEE) SEED OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, TETRAHYDRODEMETHOXYDIFERULOYLMETHANE, HYDROLYZED MILK
PROTEIN, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, LAGERSTROEMIA INDICA EXTRACT, ASCORBYL PALMITATE, RETINYL PALMITATE, DNA, PALMITOYL OLIGOPEPTIDE,ORYZANOL, PHYTOL, PANTHENOL, TOCOPHERYL ACETATE, CERAMIDE 2, PEG-10 RAPESEED STEROL, TOCOPHEROL, DIMETHICONOL, DIMETHICONE, TRIMETHYLSILOXYSILICATE, TRIBEHENIN, PEG-100 STEARATE, CAPRYLIC/CAPRIC TRIGLYCERIDE PEG-4 ESTERS, LAURETH-4, SODIUM HYDROXIDE,DISODIUM EDTA, SILICA, CARBOMER, PHOSPHORIC ACID, TETRAHYDROBISDEMETHOXYDIFERULOYLMETHANE, HEXYLENE GLYCOL, PHENOXYETHANOL, CAPRYLYL GLYCOL, PARFUM/FRAGRANCE.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of DFBimage of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0178-2	2019-11-27	C162847	48780-1	9855d018-e165-cd31-e053-dbdaa90ab51a	1bcc491a-730f-471a-9b23-86e6eab022dc
10096-0178-3	2019-11-27	C162847	48780-1	9855d018-e165-cd31-e053-dbdaa90ab51a	1bcc491a-730f-471a-9b23-86e6eab022dc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
10096-0178-1	SolutionsAgeless Results Day	50 mL in 1 JAR	CREAM	50	1
10096-0178-2	SolutionsAgeless Results Day	1 in 1 CARTON	CREAM	1	1
10096-0178-3	SolutionsAgeless Results Day	1.1 mL in 1 PACKET	CREAM	1.1	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0178	SOLUTIONS AGELESS RESULTS DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC]	1	Legacy NDC, 3 package rows	20130216_1bcc491a-730f-471a-9b23-86e6eab022dc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
AVOBENZONE	ACTIVE INGREDIENT	G63QQF2NOX	1
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OCTISALATE	ACTIVE INGREDIENT	4X49Y0596W	1
OXYBENZONE	ACTIVE INGREDIENT	95OOS7VE0Y	1
AVOBENZONE	ACTIVE MOIETY	G63QQF2NOX	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1
OCTISALATE	ACTIVE MOIETY	4X49Y0596W	1
OXYBENZONE	ACTIVE MOIETY	95OOS7VE0Y	1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Solutions Ageless Results Day
OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
OCTINOXATE
OCTISALATE
OXYBENZONE
AVOBENZONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0178	10096-0178-1, 10096-0178-2, 10096-0178-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
OXYBENZONE	95OOS7VE0Y	ACTIB
AVOBENZONE	G63QQF2NOX	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ef0f74ed-7936-4385-ae60-51ab0691f2a6			1bcc491a-730f-471a-9b23-86e6eab022dc	2013-01-23	Warnings	Exact identifier spl id: ef0f74ed-7936-4385-ae60-51ab0691f2a6 spl set id: 1bcc491a-730f-471a-9b23-86e6eab022dc

Reported adverse events (FAERS/openFDA)#

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