FDA.reportPublic FDA data

ZINC OXIDE

Manufacturer
THE AVON COMPANY | fmg Co.Ltd
Effective date
2026-06-29
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
weekly-update
Hydrated at
2026-07-17 21:41:53

Label at a glance#

ProductAVON ANEW SOLAIRE EVERYDAY MINERAL FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREEN
Active ingredientZINC OXIDE
Label structure14 sections

Indications and 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

Dosage and administration

For sunscreen use: apply liberally 15 minutes before sun exposure children under 6 months of age: ask a doctor reapply - after 40 minutes of swimming or sweating - immediately after towel drying - at least every 2 hours 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 ...

Storage and handling

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 15.52%

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

USES

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

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.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

  • apply liberally 15 minutes before sun exposure
  • children under 6 months of age: ask a doctor
  • reapply
  • - after 40 minutes of swimming or sweating
  • - immediately after towel drying
  • - at least every 2 hours

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

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, DIMETHICONE, BENZOTRIAZOLYL DODECYL P-CRESOL, CYCLOPENTASILOXANE, POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, DIPROPYLENE GLYCOL, GLYCERIN, DISTEARDIMONIUM HECTORITE, 1,2-HEXANEDIOL, ISOSTEARIC ACID, MAGNESIUM SULFATE, PANTHENOL, POLYGLYCERYL-6 POLYRICINOLEATE, DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER, NIACINAMIDE, CAPRYLIC/CAPRIC TRIGLYCERIDE, TRIETHOXYCAPRYLYLSILANE, DISTEARYLDIMONIUM CHLORIDE, MYRISTICA FRAGRANS (NUTMEG) EXTRACT, SODIUM CITRATE, TOCOPHEROL, PAEONOL, PAEONIA SUFFRUTICOSA BRANCH/FLOWER/LEAF EXTRACT.

QUESTIONS?

OTC - QUESTIONS SECTION

1-800-FOR-AVON

SPL UNCLASSIFIED SECTION

+ Hypoallergenic
+ Dermatologist-tested
+ Suitable for Sensitive Skin
+ PABA-Free
+ Alcohol-Free
+ Water-resistant (40 minutes)
+ Reef-friendly

+ Formulated without Oxybenzone and Octinoxate

www.avon.com

MADE IN KOREA
DISTR. THE AVON

COMPANY, NEW YORK, NY 10006
©2026 THE AVON COMPANY

F4792861

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCartonBottleBottleAVON

ANEW

SOLAIRE

50
SPF

EVERYDAY
MINERAL FACE

PROTECTION CREAM
BROAD SPECTRUM SPF 50

SUNSCREEN

WATER-RESISTANT (40 MINUTES)

50 ml/1.7 fl.oz.

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-212010096-2120-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
DISTEARYLDIMONIUM CHLORIDEOM9573ZX3XIACT
DIMETHICONE92RU3N3Y1OIACT
POLYGLYCERYL-6 POLYRICINOLEATEYPM0ZOC2HRIACT
SODIUM CITRATE1Q73Q2JULRIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
DIPROPYLENE GLYCOLE107L85C40IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
NUTMEGAEE24M3MQ9IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
MAGNESIUM SULFATEDE08037SABIACT
PAEONOL3R834EPI82IACT
ISOSTEARIC ACIDX33R8U0062IACT
WATER059QF0KO0RIACT
ZINC OXIDESOI2LOH54ZACTIB
DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER2P2G24V6T9IACT
NIACINAMIDE25X51I8RD4IACT
TOCOPHEROLR0ZB2556P8IACT
BENZOTRIAZOLYL DODECYL P-CRESOL298PX4M11XIACT
POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S)RLA2U05Z4QIACT
GLYCERINPDC6A3C0OXIACT
PANTHENOLWV9CM0O67ZIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-06-23monthly-update2026-07-17 21:35:36

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
AVON ANEW SOLAIRE EVERYDAY MINERAL FACE PROTECTION BROAD SPECTRUM SPF 50 SUNSCREENZINC OXIDETHE AVON COMPANY54f7c1d1-acdb-fd25-e063-6294a90a81732026-06-29WarningsExact identifier
ndc (package): 10096-2120-1
ndc (product): 10096-2120
ndc11 (package): 10096212001
spl id: 556ac858-092d-c920-e063-6294a90a8dcb
spl set id: 54f7c1d1-acdb-fd25-e063-6294a90a8173

Reported adverse events (FAERS/openFDA)#

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