Anew Ultimate

Manufacturer
Avon Products, Inc. | Avon Manufacturing (Guangzhou) Ltd
Effective date
2018-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:55:44

Label at a glance#

ProductAnew Ultimate Day Multi-Performance
Active ingredientHOMOSALATE, OCTINOXATE, OXYBENZONE, AVOBENZONE
Label structure7 sections

Storage and handling

Other Information protect the product in this container from excessive heat and direct sun product may stain certain types of fabrics

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Homosalate 8.0%............................

Octinoxate 5.0%..............................

Oxybenzone 4.0%.........................

Avobenzone 2.9%...........................

OTC - PURPOSE SECTION

Purpose

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

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

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

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

INDICATIONS & USAGE SECTION

Uses

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

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

​For sunscreen use:

  • apply liberally 15 minutes before sun exposure
  • children under 6 month of age:ask a doctor
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating
  • 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
  • product may stain certain types of fabrics

INACTIVE INGREDIENT SECTION

Inactive ingredients:

water/eau, glycerin, dimethicone, butylene glycol, glycolic acid, behenyl alcohol, hydrogenated polyisobutene, trisiloxane, ethylhexyl isononanoate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, cetearyl alcohol, isohexadecane, phytol, thiodipropionic acid, PEG-100 stearate, ammonium hydroxide, parfum/fragrance, cetearyl glucoside, phenoxyethanol, dimethiconol, polysorbate 60, disodium EDTA, PEG-150 distearate, maltodextrin, tiliacora triandra leaf/vine extract, thiazolylalanine, saccharomyces ferment lysate filtrate, eclipta prostrata extract, saccharomyces/platinum ferment, isomalt, propylene glycol, SD alcohol 40-B, saccharomyces/copper ferment, saccharomyces/magnesium ferment, saccharomyces/malachite ferment, saccharomyces/tourmaline ferment, saccharomyces/zinc ferment, steareth-20, lecithin, vitis vinifera (grape) fruit cell extract, palmitoyl tetrapeptide-10, palmitoyl tetrapeptide-7, palmitoyl lysyl aminovaleroyl lysine, caramel, red 4/CI 14700.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71110-0013-12020-01-31C16284748780-19d75b9d1-027f-f424-e053-dadaa90a57ce6d99622e-0ab4-9da2-e053-2a91aa0aceb5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71110-0013-1Anew UltimateDay Multi-Performance1.1 g in 1 PACKETCREAM1.11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71110-0013ANEW ULTIMATE DAY MULTI-PERFORMANCE (HOMOSALATE, OCTINOXATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]1Legacy NDC, 1 package rows20180601_6d99622e-0ab4-9da2-e053-2a91aa0aceb5.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71110-001371110-0013-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Source Document#

Source XML · Source PDF

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
5994a8ca-1240-cc76-e063-6394a90af94a6d99622e-0ab4-9da2-e053-2a91aa0aceb52026-08-21WarningsExact identifier
spl set id: 6d99622e-0ab4-9da2-e053-2a91aa0aceb5

Reported adverse events (FAERS/openFDA)#

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