FDA.reportPublic FDA data

Amarte ULTRA VEIL Daily

Manufacturer
Amarte USA LLC
Effective date
2025-07-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:07:21

Label at a glance#

ProductAmarte ULTRA VEIL Daily
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE, ETHYLHEXYL SALICYLATE, ETHYLHEXYL METHOXYCINNAMATE
Label structure10 sections

Dosage and administration

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 p...

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

titanium dioxide 5.0%

ethylhexyl methoxycinnamate 4.0%

ethylhexyl salicylate 4.0%

zinc oxide 3.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

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 by the sun

Warnings

WARNINGS SECTION

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.

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION


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

INACTIVE INGREDIENT SECTION

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

STORAGE AND HANDLING SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84779-115-05Amarte ULTRA VEIL Daily1 in 1 BOXLOTION12
84779-115-05Amarte ULTRA VEIL Daily5 mL in 1 BOTTLELOTION52
84779-115-70Amarte ULTRA VEIL Daily1 in 1 BOXLOTION12
84779-115-70Amarte ULTRA VEIL Daily70 mL in 1 BOTTLELOTION702

Products#

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

DailyMed product names page 1 of 2 · 41 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84779-11584779-115-70, 84779-115-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 39 matching rows.

Name, UNII, Kind table
NameUNIIKind
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
SODIUM HYALURONATEYSE9PPT4THIACT
GLYCERINPDC6A3C0OXIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
WATER059QF0KO0RIACT
PHELLINUS LINTEUS WHOLEYVO92B1UCAIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
THYMUS SERPYLLUM86H4S6K51NIACT
CAVIAR, UNSPECIFIED020K6HLU0OIACT
CAPRYLYL GLYCOL00YIU5438UIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
CITRALT7EU0O9VPPIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)V2W71V8T0XIACT
ZINC OXIDESOI2LOH54ZACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
CYCLOHEXASILOXANEXHK3U310BAIACT
NIACINAMIDE25X51I8RD4IACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
HEXYL LAURATE4CG9F9W01QIACT
ASPALATHUS LINEARIS WHOLEO17JQA1A9ZIACT
GINKGO BILOBA SEED8CQ734K3W7IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
LINALOOLD81QY6I88EIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SULFUR70FD1KFU70IACT
GERANIOLL837108USYIACT
MAGNESIUM SULFATE, UNSPECIFIEDDE08037SABIACT
STEARIC ACID4ELV7Z65APIACT
ADENOSINEK72T3FS567IACT
ETHYLHEXYL SALICYLATE4X49Y0596WACTIB
COPTIS JAPONICA WHOLE8BO3NHJ535IACT
POTENTILLA ERECTA ROOTBI896CKT6BIACT
SH-OLIGOPEPTIDE-1TZK30RF92WIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
LIMONENE, (+)-GFD7C86Q1WIACT
ETHYLHEXYL METHOXYCINNAMATE4Y5P7MUD51ACTIB

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
Amarte ULTRA VEIL DailySUNSCREENAmarte USA LLC39e9ca98-d0e8-6b8f-e063-6394a90aa3662025-07-15WarningsExact identifier
ndc (package): 84779-115-05
ndc (package): 84779-115-70
ndc (product): 84779-115
ndc11 (package): 84779011570
ndc11 (package): 84779011505
spl id: 3a017a63-4a10-f57e-e063-6394a90ab7bb
spl set id: 39e9ca98-d0e8-6b8f-e063-6394a90aa366

Reported adverse events (FAERS/openFDA)#

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