AMARTE ULTRA VEIL DAILY- sunscreen lotion

Amarte ULTRA VEIL Daily by

Drug Labeling and Warnings

Amarte ULTRA VEIL Daily by is a Otc medication manufactured, distributed, or labeled by Amarte USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

titanium dioxide 5.0%

ethylhexyl methoxycinnamate 4.0%

ethylhexyl salicylate 4.0%

zinc oxide 3.0%

Purpose

Sunscreen

Use

■ 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

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.

WHEN USING

keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

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

Directions

Directions ■ shake well ■ apply liberally 15 minutes before sun exposure ■ use a water-resistant product if swimming or sweating ■ reapply at least every 2 hours ■ children under 6 months: ask a doctor ■ 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 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-sleeve shirts, pants, hats, and sunglasses

Inactive ingredients

water, cyclopentasiloxane, caprylic/capric triglyceride, butylene glycol, cyclohexasiloxane, niacinamide, PEG-10 dimethicone, cetyl PEG/PPG-10/1 dimethicone, sorbitan sesquioleate, hexyl laurate, magnesium sulfate, sodium hyaluronate, glycerin, Aspalathus linearis extract, Ginkgo biloba nut extract, Coptis japonica extract, Scutellaria baicalensis root extract, Potentilla erecta root extract, Phellinus linteus extract, Thymus serpyllum extract, caviar extract, adenosine, sh-oligopeptide-1, caprylyl glycol, ethylhexylglycerin, 1,2-hexanediol, stearic acid, triethoxycaprylylsilane, aluminum hydroxide, phenoxyethanol, sulfur, limonene, linalool, geraniol, citral, fragrance

Other information

■ protect the product in this container from excessive heat and direct sun

QUESTIONS

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

AMARTE ULTRA VEIL DAILY 
sunscreen lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84779-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	50 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	30 mg  in 1 mL
ETHYLHEXYL SALICYLATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	ETHYLHEXYL SALICYLATE	40 mg  in 1 mL
ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51) (ETHYLHEXYL METHOXYCINNAMATE - UNII:4Y5P7MUD51)	ETHYLHEXYL METHOXYCINNAMATE	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
GLYCERIN (UNII: PDC6A3C0OX)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
WATER (UNII: 059QF0KO0R)
PHELLINUS LINTEUS WHOLE (UNII: YVO92B1UCA)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
THYMUS SERPYLLUM (UNII: 86H4S6K51N)
CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CITRAL (UNII: T7EU0O9VPP)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOHEXASILOXANE (UNII: XHK3U310BA)
NIACINAMIDE (UNII: 25X51I8RD4)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
ASPALATHUS LINEARIS WHOLE (UNII: O17JQA1A9Z)
GINKGO BILOBA SEED (UNII: 8CQ734K3W7)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
LINALOOL (UNII: D81QY6I88E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SULFUR (UNII: 70FD1KFU70)
GERANIOL (UNII: L837108USY)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
STEARIC ACID (UNII: 4ELV7Z65AP)
ADENOSINE (UNII: K72T3FS567)
COPTIS JAPONICA WHOLE (UNII: 8BO3NHJ535)
POTENTILLA ERECTA ROOT (UNII: BI896CKT6B)
SH-OLIGOPEPTIDE-1 (UNII: TZK30RF92W)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
LIMONENE, (+)- (UNII: GFD7C86Q1W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84779-115-70	1 in 1 BOX	07/15/2025
1		70 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 84779-115-05	1 in 1 BOX	07/15/2025
2		5 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/15/2025

Labeler - Amarte USA LLC (119352166)