FDA.reportPublic FDA data

Avon Nutra Effects

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#

ProductAvon Nutra Effects Hydration Day Cream
Active ingredientOCTINOXATE, HOMOSALATE, AVOBENZONE, OXYBENZONE
Label structure12 sections

Storage and handling

Other Information Protect the product in this container from excessive heat and direct sun, Product may stain fabrics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Octinoxate 5.5%......

Homosalate 5.0%....

Avonbenzone 2.9%.....

Oxybenzone 1.0%......

OTC - PURPOSE SECTION

Purpose

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

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

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

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

INDICATIONS & USAGE SECTION

Uses

Helps prevent sunburn.

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 our of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

For suncreen use:

Apply liberally 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.
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-procteion measures, including:
Limite time in the sun, expecially 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 fabrics.

INACTIVE INGREDIENT SECTION

Inactive ingredients

WATER/EAU, GLYCERIN, PROPANEDIOL, DIMETHICONE, HYDROGENATED POLYISOBUTENE, HYDROXYETHYL UREA, LAURYL LACTATE, CETEARYL ALCOHOL, SILICA, PEG-100 STEARATE, PENTYLENE GLYCOL, FRAGRANCE/PARFUM, PHENOXYETHANOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CETEARETH-20, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, CARBOMER, CHLORPHENESIN, DISODIUM EDTA, ISOHEXADECANE, ETHYLENE/PROPYLENE/STYRENE COPOLYMER, UREA, CHOLESTEROL, DILAURYL THIODIPROPIONATE, DIMETHICONE CROSSPOLYMER, PHYTOL, SODIUM HYDROXIDE, XANTHAN GUM, SODIUM DEHYDROACETATE, SODIUM PCA, POLYSORBATE 60, PANTHENOL, BORON NITRIDE, SODIUM HYALURONATE, TOCOPHERYL ACETATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, BUTYLENE/ETHYLENE/STYRENE COPOLYMER,

HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, CEREUS GRANDIFLORUS (CACTUS) FLOWER EXTRACT, SALVIA HISPANICA SEED EXTRACT, MALTODEXTRIN, POUZOLZIA PENTANDRA EXTRACT, PELVETIA CANALICULATA EXTRACT.

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
71110-0012-12020-01-31C16284748780-19d75b9d0-ab6d-f424-e053-dadaa90a57ce6d9779cf-907e-2696-e053-2991aa0a9a91

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71110-0012-1Avon Nutra EffectsHydration Day Cream1.1 g in 1 PACKETCREAM1.11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71110-0012AVON NUTRA EFFECTS HYDRATION DAY CREAM (OCTINOXATE, HOMOSALATE, AVONBENZONE, OXYBENZONE) CREAM [AVON PRODUCTS, INC.]1Legacy NDC, 1 package rows20180601_6d9779cf-907e-2696-e053-2991aa0a9a91.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71110-001271110-0012-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
DILAURYL THIODIPROPIONATEV51YH1B080IACT
SODIUM DEHYDROACETATE8W46YN971GIACT
POLYSORBATE 60CAL22UVI4MIACT
BORON NITRIDE2U4T60A6YDIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
ISOHEXADECANE918X1OUF1EIACT
CHOLESTEROL97C5T2UQ7JIACT
PANTHENOLWV9CM0O67ZIACT
MALTODEXTRIN7CVR7L4A2DIACT
OCTINOXATE4Y5P7MUD51ACTIB
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
OXYBENZONE95OOS7VE0YACTIB
PHYTOL5BC2RZ81NGIACT
SODIUM HYDROXIDE55X04QC32IIACT
XANTHAN GUMTTV12P4NEEIACT
PENTYLENE GLYCOL50C1307PZGIACT
DIMETHICONE92RU3N3Y1OIACT
HYDROXYETHYL UREAMBQ7DDQ7ARIACT
LAURYL LACTATEG5SU0BFK7OIACT
PEG-100 STEARATEYD01N1999RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CHLORPHENESINI670DAL4SZIACT

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
59949f0b-c64a-c29c-e063-6394a90a93066d9779cf-907e-2696-e053-2991aa0a9a912026-08-21WarningsExact identifier
spl set id: 6d9779cf-907e-2696-e053-2991aa0a9a91

Reported adverse events (FAERS/openFDA)#

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