FACE

Manufacturer
AGEFARM SRL | COSMESIT SRL
Effective date
2019-09-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:12:50

Label at a glance#

ProductFACE SPF 50
Active ingredientOCTOCRYLENE, OXYBENZONE, AVOBENZONE, OCTINOXATE, TITANIUM DIOXIDE
Label structure8 sections

Indications and uses

helps prevent sunburn use as directed with other sun protection measures (see Direction), decrease the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

apply liberally 15 minutes before sun exposure reapply: at least every 2 hours, immediately after towel drying use a water-resistant sunscreen if swimming or sweating children under 6 months: Ask a doctor Sun Protection Measures. Spending time in the sun increases your risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including: limite the time in the...

Storage and handling

Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

Drug Facts Active ingredients

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE 2%

OCTINOXATE 2%

OCTOCRYLENE 2%

OXYBENZONE 2%

TITANIUM DIOXIDE 2%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

helps prevent sunburn

use as directed with other sun protection measures (see Direction), decrease the risk of skin cancer and early skin aging caused by the sun

WARNINGS

WARNINGS AND PRECAUTIONS SECTION

For external use only

Do not use on damaged or broken skin

Stop use and ask doctor if rash occurs

When using this product, keep put of eyes. Rinse with water to remove

Keep out of reach of children. If swalloed, get medical help or contact Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

apply liberally 15 minutes before sun exposure

reapply: at least every 2 hours, immediately after towel drying

use a water-resistant sunscreen if swimming or sweating

children under 6 months: Ask a doctor

Sun Protection Measures. Spending time in the sun increases your risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including:

limite the time in the sun, especially from 10 a.m. - 2 p.m.

wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ammonium acryloydimethytaurate-vp copolymer, bis-ethylhexyloxphenol methoxphenyl triazine, BHT, butyrospermum parkii butter extract, caprylic capric triglyceride, carbomer, carthamus, cetearyl alcohol, citronellol,coumarin, diethylhexylsyringylidenemalonate, decyl gluside, diisopropyl sebacate, dimethicone, dimethiconol behenate, c12-15 alkyl benzoate, glycerin, glyceryl stearate, hexyl cinnamal, hydrolyzed soy protein, hydrolyzed wheat protein, limanathes alba seed oil, limonene, linalool, methylene bisbenzotriazolyl tetramethybutyphenol (nano), menthyl lactate, methylisothiazolinone, olea europapea oil unasonifiables, parfum, peg-100 stearate, phenoxyethanol, pseudoalteromonas ferment extract, propylene glycol, tocopherylacetate, triethanolamine, tripeptide-1, tripeptide-10 citrulline, vp-eicosene copolymer, water, xanthan gum

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun

SUNSCREEN LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sunscreen 5022 spf 50.jpgsunscreen 5022 spf 50.jpgSUNSCREEN FACE SPF 50 SPRAY 5022

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73310-5022-22025-04-16C16284748780-1ba0f9c33-1398-a910-e053-dadaa90a0b85SUNSCREEN Face SPF 50
73310-5022-22021-01-29C16284748780-1ba0f9c33-1398-a910-e053-dadaa90a0b85SUNSCREEN Face SPF 50

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73310-502273310-5022-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
32e6b134-939b-483e-e063-6394a90ae30f90d3e398-a820-1608-e053-2a95a90ab3182025-04-16WarningsExact identifier
spl set id: 90d3e398-a820-1608-e053-2a95a90ab318

Reported adverse events (FAERS/openFDA)#

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