Nutra Effects Balance Day Cream SPF15
- Manufacturer
- New Avon LLC
- Effective date
- 2018-04-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 22:55:07
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active Ingredients/Ingrédients actifs:
OCTINOXATE (5.5 %), HOMOSALATE (5.0 %), AVOBENZONE (2.9 %), OXYBENZONE (1.0 %).
INDICATIONS & USAGE
Uses
- helps prevent sunburn
WARNINGS
For external use only
Do not use on damaged or broken skin
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION
Directions
- For sunscreen use:
- apply generously 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 protection measures including:
- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
Other Information
- protect the product in this container from excessive heat and direct sun
- product may stain fabrics
INACTIVE INGREDIENT
Inactive Ingredients/Ingrédients inactifs: WATER/EAU, BUTYLENE GLYCOL, DIMETHICONE, ETHYLHEXYL ISONONANOATE, PEG-8, SILICA, GLYCERIN, POLYSILICONE-11, CAPRYLYL GLYCOL, PARFUM/FRAGRANCE, GLYCERYL STEARATE, HYDROGENATED LECITHIN, PHENOXYETHANOL, BEHENYL ALCOHOL, CETYL ALCOHOL, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, DISODIUM EDTA, PANTHENOL, TALC, CHOLETH-24, ISOHEXADECANE, SODIUM HYDROXIDE, HEXYLENE GLYCOL, CETETH-24, POLYGLYCERYL-3 DIISOSTEARATE, PYRIDOXINE HCL, POLYSORBATE 60, LAURETH-12, TOCOPHERYL ACETATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, PHYTOL, ISOMALT, MALTODEXTRIN, POUZOLZIA PENTANDRA EXTRACT, SALVIA HISPANICA SEED EXTRACT, LECITHIN, VITIS VINIFERA (GRAPE) FRUIT CELL EXTRACT.
QUESTIONS
Questions or Comments?
Call toll free
1-800-FOR-AVON or
1-800-265-AVON in Canada
PACKAGE LABEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10096-9502-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-d53a-f424-e053-dadaa90a57ce | Nutra Effects Balance Day Cream SPF15 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10096-9502-1 | Nutra Effects Balance Day Cream SPF15 | 50 g in 1 JAR | CREAM | 50 | 2 | |
| 10096-9502-2 | Nutra Effects Balance Day Cream SPF15 | 1 in 1 CARTON | CREAM | 1 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10096-9502 | NUTRA EFFECTS BALANCE DAY CREAM SPF15 CREAM [NEW AVON LLC] | 2 | Legacy NDC, 2 package rows | 20180402_68c6a717-ebc5-28b9-e053-2a91aa0acb61.zip |
Products#
Every source-derived product name is available through these pages.
- Nutra Effects Balance Day Cream SPF15
- WATER
- OCTINOXATE
- OXYBENZONE
- HOMOSALATE
- AVOBENZONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10096-9502 | 10096-9502-1, 10096-9502-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| OCTINOXATE | 4Y5P7MUD51 | ACTIB |
| OXYBENZONE | 95OOS7VE0Y | ACTIB |
| HOMOSALATE | V06SV4M95S | ACTIB |
| AVOBENZONE | G63QQF2NOX | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 68dec142-698c-5afc-e053-2991aa0a65ed | 68c6a717-ebc5-28b9-e053-2a91aa0acb61 | 2018-04-02 | Warnings | 68dec142-698c-5afc-e053-2991aa0a65ed 68c6a717-ebc5-28b9-e053-2a91aa0acb61 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
