Sun Veil IlluminatingElixir Face Sunscreen SPF 38

Manufacturer
Koco Life LLC | PhytogenX, Inc.
Effective date
2026-02-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:36:48

Label at a glance#

ProductSun Veil IlluminatingElixir Face Sunscreen SPF 38
Active ingredientOCTISALATE, OCTOCRYLENE, ZINC OXIDE
Label structure9 sections

Indications and uses

• Helps prevent sunburn • If used as directed with other sun protectionmeasures (see Directions), decreases the riskof skin cancer and early skin aging causedby the sun

Dosage and administration

• Apply generously & evenly 15 minutes before sun exposure. 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...

Storage and handling

Protect the product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octisalate 5%

Octocrylene 10%

Zinc Oxide 15%

Purpose

OTC - PURPOSE SECTION

Octisalate 5%.......................................Sunscreen

Octocrylene 10%..................................Sunscreen

Zinc Oxide 15%.....................................Sunscreen

Uses

INDICATIONS & USAGE SECTION

• Helps prevent sunburn

• If used as directed with other sun protectionmeasures (see Directions), decreases the riskof skin cancer and early skin aging causedby 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 product is swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply generously & evenly 15 minutes before sun exposure.

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. • Wearlong-sleeved shirts, pants, hats, and sunglasses.

• Children under 6 months: Ask doctor

Other information

STORAGE AND HANDLING SECTION

Protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Butyloctyl Salicylate, Polyglyceryl-3 Polyricinoleate, Propanediol, Sodium Chloride, Caprylic/Capric Triglyceride, Mica, Niacinamide, Sodium Hyaluronate, Panthenol, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantifolia (Lime) Oil, Tocopherol, 1,2-Hexanediol, Styrene/MA Copolymer, Ethylhexylglycerin, Triethyl Citrate, Xanthan Gum, Maltol, Dimethyl Heptenal, Gamma-Decalactone, Geraniol, Geranyl Acetate, 3,6-Nonadienol, Terpineol, Hexyl Acetate, Ethyl Butyrate, Benzyl Alcohol, Limonene, Citrus Aurantium Peel Oil, Sodium Hydroxide, Tin Oxide,Sodium Ferrocyanide, Iron Titanium Oxide, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491), Iron Oxides (CI 77499).

Questions or comments?

OTC - QUESTIONS SECTION

Call (858) 252-0099

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kopari

Sun Veil Illuminating Elixir Face Sunscreen

SPF 38

1 Fl. Oz. | 30 mL

11

22

33

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850068900909GTIN-13: 0850068900909
EAN-13: 0850068900909
GTIN-12: 850068900909
UPC-A: 850068900909
GTIN storage (14 digits): 00850068900909
Screenshot 2026-02-05 092639.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84130-019-11Sun Veil IlluminatingElixir Face Sunscreen SPF 3830 mL in 1 BOTTLE, DROPPERLOTION301
84130-019-12Sun Veil IlluminatingElixir Face Sunscreen SPF 381 in 1 CARTONLOTION11
84130-019-20Sun Veil IlluminatingElixir Face Sunscreen SPF 388 mL in 1 TUBELOTION81

Products#

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

DailyMed product names page 1 of 2 · 43 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84130-01984130-019-11, 84130-019-12, 84130-019-20

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 41 matching rows.

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sun Veil IlluminatingElixir Face Sunscreen SPF 38OCTISALATE, OCTOCRYLENE, ZINC OXIDEKoco Life LLC4a15c479-d676-9e52-e063-6394a90a4eb42026-02-05WarningsExact identifier
ndc (package): 84130-019-11
ndc (package): 84130-019-20
ndc (package): 84130-019-12
ndc (product): 84130-019
ndc11 (package): 84130001911
ndc11 (package): 84130001920
ndc11 (package): 84130001912
spl id: 4a15c479-d677-9e52-e063-6394a90a4eb4
spl set id: 4a15c479-d676-9e52-e063-6394a90a4eb4
Glow This WayOCTISALATE, OCTOCRYLENE, ZINC OXIDE, AVOBENZONE, HOMOSALATEKoco Life LLC4619cf96-987a-3e88-e063-6294a90afbe92026-01-15WarningsExact identifier
ndc (package): 84130-019-11
ndc11 (package): 84130001911

Reported adverse events (FAERS/openFDA)#

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