SUN VEIL ILLUMINATINGELIXIR FACE SUNSCREEN SPF 38- octisalate, octocrylene, zinc oxide lotion

Sun Veil IlluminatingElixir Face Sunscreen SPF 38 by

Drug Labeling and Warnings

Sun Veil IlluminatingElixir Face Sunscreen SPF 38 by is a Otc medication manufactured, distributed, or labeled by Koco Life LLC, PhytogenX, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Octisalate 5%

Octocrylene 10%

Zinc Oxide 15%

Purpose

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

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

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

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

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

Directions

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

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

Inactive ingredients

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?

Call (858) 252-0099

PRINCIPAL DISPLAY PANEL

Kopari

Sun Veil Illuminating Elixir Face Sunscreen

SPF 38

1 Fl. Oz. | 30 mL

INGREDIENTS AND APPEARANCE

SUN VEIL ILLUMINATINGELIXIR FACE SUNSCREEN SPF 38 
octisalate, octocrylene, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84130-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	150 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM FERROCYANIDE (UNII: 5HT6X21AID)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
CI 77491 (UNII: 1K09F3G675)
CI 77499 (UNII: XM0M87F357)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
3,6-NONADIEN-1-OL, (3Z,6Z)- (UNII: 8J66AVE64W)
CITRUS AURANTIUM PEEL OIL (UNII: 9TLV70SV6I)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
CITRUS AURANTIFOLIA (LIME) OIL (UNII: UZH29XGA8G)
DIMETHYL HEPTENAL (UNII: Z331YX9EL9)
HEXYL ACETATE (UNII: 7U7KU3MWT0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MICA (UNII: V8A1AW0880)
TERPINEOL (UNII: R53Q4ZWC99)
LITSEA CUBEBA FRUIT OIL (UNII: 2XIW34BN6O)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ETHYL BUTYRATE (UNII: UFD2LZ005D)
TIN OXIDE (UNII: KM7N50LOS6)
TOCOPHEROL (UNII: R0ZB2556P8)
MALTOL (UNII: 3A9RD92BS4)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
MENTHA VIRIDIS (SPEARMINT) LEAF OIL (UNII: C3M81465G5)
GERANYL ACETATE (UNII: 3W81YG7P9R)
NIACINAMIDE (UNII: 25X51I8RD4)
BENZYL ALCOHOL (UNII: LKG8494WBH)
FERRIC TITANATE (UNII: SNK8ZSY7RU)
PANTHENOL (UNII: WV9CM0O67Z)
XANTHAN GUM (UNII: TTV12P4NEE)
GAMMA-DECALACTONE (UNII: 7HLS05KP9O)
CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL (UNII: AKN3KSD11B)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
GERANIOL (UNII: L837108USY)
PROPANEDIOL (UNII: 5965N8W85T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84130-019-12	1 in 1 CARTON	01/15/2026
1	NDC: 84130-019-11	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2	NDC: 84130-019-20	8 mL in 1 TUBE; Type 0: Not a Combination Product	01/15/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/15/2026

Labeler - Koco Life LLC (046650159)

Establishment
Name	Address	ID/FEI	Business Operations
PhytogenX, Inc.		624386772	manufacture(84130-019)