Anew Clinical

Manufacturer
New Avon LLC | Avon Products, Inc
Effective date
2016-03-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:45:18

Label at a glance#

ProductAnew Clinical Absolute Even Spot Correcting Hand
Active ingredientoctinoxate, oxybenzone, 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 ingredientsOCTINOXATE 7.5%, OXYBENZONE 4.0%,
AVOBENZONE 2.0%.......................

OTC - PURPOSE SECTION

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

• 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

• 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, GLYCERIN, PENTAERYTHRITYL TETRAETHYLHEXANOATE, STEARETH-2, GLYCOLIC ACID, BEHENYL ALCOHOL, DIMETHICONE, PEG-40 STEARATE, MYRISTYL MYRISTATE, TRISILOXANE, LAURYL LACTATE, ASPARTIC ACID, ZEA MAYS (CORN) KERNEL EXTRACT, PHYTOL, BUTYROSPERMUM PARKII (SHEA) BUTTER, COLA NITIDA SEED EXTRACT, GLYCINE SOJA (SOYBEAN) SEED EXTRACT, PUNICA GRANATUM FRUIT JUICE, RETINYL PALMITATE, DAUCUS CAROTA SATIVA (CARROT) ROOT EXTRACT, ASCORBYL PALMITATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, RETINOL, GLYCINE SOJA (SOYBEAN) OIL, SAXIFRAGA SARMENTOSA EXTRACT, VITIS VINIFERA (GRAPE) FRUIT EXTRACT, TOCOPHEROL, BETA-CAROTENE, MORUS NIGRA ROOT EXTRACT, SCUTELLARIA BAICALENSIS ROOT EXTRACT, GLYCERYL STEARATE, PEG-100 STEARATE, PVM/MA DECADIENE CROSSPOLYMER, XANTHAN GUM, SILICA, ACRYLATES/CARBAMATE COPOLYMER, MALTODEXTRIN, LECITHIN, TRIMETHYLSILOXYSILICATE, BUTYLENE GLYCOL, AMMONIUM HYDROXIDE, PHENOXYETHANOL, METHYLPARABEN, DISODIUM EDTA, BHT, PARFUM/FRAGRANCE.

OTC - QUESTIONS SECTION

Questions? 1-800-FOR-AVON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDP
image of PDP
image of DFB
image of DFB
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0290-22020-01-31C16284748780-19d75b9d0-8b09-f424-e053-dadaa90a57ced15fcfb4-e300-4f7e-8ec4-7ed1d0101c2f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0290-1Anew ClinicalAbsolute Even Spot Correcting Hand75 g in 1 TUBECREAM753
10096-0290-2Anew ClinicalAbsolute Even Spot Correcting Hand1 in 1 CARTONCREAM13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0290ANEW CLINICAL ABSOLUTE EVEN SPOT CORRECTING HAND (OCTINOXATE, OXYBENZONE, AVOBENZONE) CREAM [NEW AVON LLC]3Legacy NDC, 2 package rows20160303_d15fcfb4-e300-4f7e-8ec4-7ed1d0101c2f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
avobenzoneACTIVE INGREDIENTG63QQF2NOX1
octinoxateACTIVE INGREDIENT4Y5P7MUD511
oxybenzoneACTIVE INGREDIENT95OOS7VE0Y1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OXYBENZONEACTIVE MOIETY95OOS7VE0Y1

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
10096-029010096-0290-1, 10096-0290-2

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
oxybenzone95OOS7VE0YACTIB
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
f103ab6a-a5a4-4e0d-bd3e-420b0ecc3d7ad15fcfb4-e300-4f7e-8ec4-7ed1d0101c2f2016-03-01WarningsExact identifier
spl id: f103ab6a-a5a4-4e0d-bd3e-420b0ecc3d7a
spl set id: d15fcfb4-e300-4f7e-8ec4-7ed1d0101c2f

Reported adverse events (FAERS/openFDA)#

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