ultra color absolute

Manufacturer: New Avon LLC | Avon Cosmetics Manofacturing, S. de R.L. de C.V.
Effective date: 2016-02-19
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:45:17

Label at a glance#

Productultra color absolute

Active ingredientOCTINOXATE

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

PhoneLabel contact1-800-265-AVON

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Octinoxate 7.5%.............................................

OTC - PURPOSE SECTION

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

For sunscreen use:
• 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:
DIISOPROPYL DIMER DILINOLEATE, LANOLIN, DI-PPG-3 MYRISTYL ETHER ADIPATE, TRIDECYL TRIMELLITATE, SYNTHETIC WAX, POLYBUTENE, STEARYL/PPG-3 MYRISTYL ETHER DIMER DILINOLEATE, SILICA, MICROCRYSTALLINE WAX/CIRE MICROCRISTALLINE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, DIPHENYL DIMETHICONE, PHENYL TRIMETHICONE, OZOKERITE, DILAURYL THIODIPROPIONATE, GLYCERIN, LAURYL PCA, NYLON-12, PHYTOL, TOCOPHERYL ACETATE, CAPRYLYL GLYCOL, DISTEARDIMONIUM HECTORITE, DIPALMITOYL HYDROXYPROLINE, ETHYLENE/
PROPYLENE/STYRENE COPOLYMER, TRIETHYL CITRATE, ACRYLATES COPOLYMER, PARFUM/FRAGRANCE, ACRYLATES/CARBAMATE COPOLYMER, PALMITIC ACID, C12-15 ALKYL BENZOATE, WATER/EAU, DIMETHICONE, COLLAGEN, TRIBEHENIN, BUTYLENE/ETHYLENE/STYRENE COPOLYMER,
SACCHARIN, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, CERAMIDE 2, PEG-10 RAPESEED STEROL, CAMELLIA SINENSIS LEAF EXTRACT, ASCORBIC ACID, BUTYROSPERMUM PARKII (SHEA) BUTTER, SILICA DIMETHYL SILYLATE, BEESWAX/CIRE D’ABEILLE, POLYESTER-1, PALMITOYL OLIGOPEPTIDE, PEG-200. SHIMMER SHADES MAY ALSO CONTAIN: CALCIUM SODIUM BOROSILICATE, BARIUM SULFATE, TIN OXIDE. MAY CONTAIN: RED 7 LAKE/CI 15850, TITANIUM DIOXIDE/CI 77891, RED 6 LAKE/CI 15850, IRON OXIDES, MICA/CI 77019, YELLOW 5 LAKE/CI 19140, YELLOW 6 LAKE/CI 15985, BLUE 1 LAKE/CI 42090, RED 33 LAKE/CI 17200, RED 27 LAKE/CI 45410, CARMINE/CI 75470.

OTC - QUESTIONS SECTION

Questions or Comments?
Call toll free 1-800-FOR-AVON or 1-800-265-AVON in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of cartonimage of cartonimage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0325-2	2020-01-31	C162847	48780-1	9d75b9d0-e230-f424-e053-dadaa90a57ce	91e56b45-d96d-4a03-baee-043af451b68f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0325-1	ultra color absolute	3 g in 1 PACKAGE	LIPSTICK	3		2
10096-0325-2	ultra color absolute	1 in 1 CARTON	LIPSTICK	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0325	ULTRA COLOR ABSOLUTE (OCTINOXATE) LIPSTICK [NEW AVON LLC]	2	Legacy NDC, 2 package rows	20160303_91e56b45-d96d-4a03-baee-043af451b68f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

ultra color absolute
Octinoxate

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0325	10096-0325-1, 10096-0325-2

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	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
00b51523-cb2d-4242-aae7-345da33161a3			91e56b45-d96d-4a03-baee-043af451b68f	2016-02-19	Warnings	Exact identifier spl id: 00b51523-cb2d-4242-aae7-345da33161a3 spl set id: 91e56b45-d96d-4a03-baee-043af451b68f

Reported adverse events (FAERS/openFDA)#

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