Storage and handling
Other Information Protect the product in this container from excessive heat and direct sun, Product may stain fabrics.
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 22:55:45
Label at a glance#
ProductAvon Nutra Effects Radiance Day Cream
Active ingredientOCTINOXATE, HOMOSALATE, AVOBENZONE, OXYBENZONE
Label structure12 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active Ingredients:
OCTINOXATE 7.5 % ……………………………
OXYBENZONE 3.5 % ……………………………
HOMOSALATE 3.0 % ………………………………
AVOBENZONE 2.5 % ……………………………
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, DIMETHICONE, GLYCERIN, PEG-8, CETEARYL ALCOHOL, TRISILOXANE, BEHENYL ALCOHOL, BUTYLOCTYL SALICYLATE, DILAURYL THIODIPROPIONATE, SILICA, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, DIMETHICONE CROSSPOLYMER, CARBOMER, CETEARETH-20, THIODIPROPIONIC ACID, PHENOXYETHANOL, SODIUM HYDROXIDE, ISOHEXADECANE, CHLORPHENESIN, DISODIUM EDTA, KAEMPFERIA GALANGA ROOT EXTRACT, PARFUM/FRAGRANCE, SODIUM DEHYDROACETATE, POLYSORBATE 60, PANTHENOL, STRELITZIA NICOLAI SEED ARIL EXTRACT, TOCOPHERYL ACETATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, SALVIA HISPANICA SEED EXTRACT, MALTODEXTRIN, POUZOLZIA PENTANDRA EXTRACT.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71110-0014-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-fab5-f424-e053-dadaa90a57ce | 6d99d58a-06e6-8b87-e053-2991aa0aff80 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71110-0014-1 | Avon Nutra EffectsRadiance Day Cream | 1.1 g in 1 PACKET | CREAM | 1.1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71110-0014 | AVON NUTRA EFFECTS RADIANCE DAY CREAM (OCTINOXATE, OXYBENZONE, HOMOSALATE, AVONBENZONE) CREAM [AVON PRODUCTS, INC.] | 1 | Legacy NDC, 1 package rows | 20180602_6d99d58a-06e6-8b87-e053-2991aa0aff80.zip |
Products#
Every source-derived product name is available through these pages.
- Avon Nutra Effects Radiance Day Cream
- Octinoxate, Oxybenzone, Homosalate, Avonbenzone
- DILAURYL THIODIPROPIONATE
- SODIUM DEHYDROACETATE
- POLYSORBATE 60
- WATER
- GLYCERIN
- ISOHEXADECANE
- PANTHENOL
- MALTODEXTRIN
- SODIUM HYDROXIDE
- DIMETHICONE
- PHENOXYETHANOL
- CHLORPHENESIN
- OCTINOXATE
- HOMOSALATE
- AVOBENZONE
- OXYBENZONE
- THIODIPROPIONIC ACID
- TRISILOXANE
- BUTYLOCTYL SALICYLATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71110-0014 | 71110-0014-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DILAURYL THIODIPROPIONATE | V51YH1B080 | IACT |
| SODIUM DEHYDROACETATE | 8W46YN971G | IACT |
| POLYSORBATE 60 | CAL22UVI4M | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ISOHEXADECANE | 918X1OUF1E | IACT |
| PANTHENOL | WV9CM0O67Z | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| DIMETHICONE | 92RU3N3Y1O | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| CHLORPHENESIN | I670DAL4SZ | IACT |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| HOMOSALATE | V06SV4M95S | ACTIB |
| AVOBENZONE | G63QQF2NOX | ACTIB |
| OXYBENZONE | 95OOS7VE0Y | ACTIB |
| THIODIPROPIONIC ACID | 3BBK323ED8 | IACT |
| TRISILOXANE | 9G1ZW13R0G | IACT |
| BUTYLOCTYL SALICYLATE | 2EH13UN8D3 | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5994b7f7-02bb-d716-e063-6394a90ab834 | 6d99d58a-06e6-8b87-e053-2991aa0aff80 | 2026-08-21 | Warnings | 6d99d58a-06e6-8b87-e053-2991aa0aff80 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.