FDA.reportPublic FDA data

Vertra Element Resistance Daily Driver

Manufacturer
EAi-JR286, INC
Effective date
2021-12-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:23:29

Label at a glance#

ProductVertra Element Resistance Daily Driver SPF30
Active ingredientHOMOSALATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE
Label structure6 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 byt the sun

Dosage and administration

Apply Liberally 15 minutes before sun exposure Reapply:    after 80 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 15 or higher and other sun protection measuers including    limit...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

  Homosalate  5%

Octisalate  5%

Avobenzone 3%

Octocrylene 2.7%

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 byt the sun

Warnings

WARNINGS SECTION

For External Use only

Do Not Use

OTC - DO NOT USE SECTION

on damaged or broken skin

When Using this product

OTC - WHEN USING SECTION

keep out of eyes

Rinse with water to remove

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs

Keep Out of reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Apply Liberally 15 minutes before sun exposure

Reapply:

   after 80 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 15 or higher and other sun protection measuers including

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

   wear long-sleeve shirts, pants, hats and sunglasses

   Children under 6 months: Ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera) Leaf Juice, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Butylene Glycol, Caprylyl Glycol, Cetearyl Alcohol, Chlorphenesin, Citrus Sinensis (Blood Orange) Fruit Extract, Coco Caprylate/Caprate, Decyl Glucoside, Dextrin, Dimethicone, Disodium EDTA, Ethylhexyl Stearate, Fragrance, Glycerin, Glyceryl Stearate,
Hydrolyzed Hibiscus Esculentus Extract, Isododecane, PEG-100 Stearate, Pentylene Glycol, Phenoxyethanol, Polysilicone-11, Polyurethane-34, Sodium Citrate, Sodium Polyacrylate, Tapioca Starch Polymethylsilsesquioxane, Tocopheryl Acetate, Trideceth 6, Water,
Xanthan Gum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyDriverDailyDriver

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71014-37171014-371-01, 71014-371-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTOCRYLENE5A68WGF6WMACTIB
ALOE VERA WHOLEKIZ4X2EHYXIACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATEKBC00G95HIIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CHLORPHENESINI670DAL4SZIACT
CITRUS SINENSIS FRUIT OILWV48LBL15QIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
DEXTRIN PALMITATE (CORN; 20000 MW)89B2BSF9I3IACT
DIMETHICONE92RU3N3Y1OIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
ABELMOSCHUS ESCULENTUS WHOLE505GKC6541IACT
ISODODECANEA8289P68Y2IACT
PEG-100 STEARATEYD01N1999RIACT
PENTYLENE GLYCOL50C1307PZGIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYURETHANE-34 (40 MPA, TENSILE STRENGTH OF FILM AT BREAK)77KA3O6NNFIACT
SODIUM CITRATE1Q73Q2JULRIACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
STARCH, TAPIOCA24SC3U704IIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
TRIDECETH-63T5PCR2H0CIACT
water059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT

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
fcae1456-2981-4d33-9e04-78802a226d4e3cac278e-459c-44ec-8044-5b27632e4bad2021-12-10WarningsExact identifier
spl id: fcae1456-2981-4d33-9e04-78802a226d4e
spl set id: 3cac278e-459c-44ec-8044-5b27632e4bad

Reported adverse events (FAERS/openFDA)#

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