FDA.reportPublic FDA data

Glint Aura Make Keep Chiffon Base Pink Beige

Manufacturer
Martble, Inc. | Aura Cosmetics Inc.
Effective date
2020-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:25:21

Label at a glance#

ProductGlint Aura Make Keep Chiffon Base Pink Beige
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure11 sections

Dosage and administration

apply liberally before sun exposure and as needed children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 5.58%

Zinc Oxide 10.36%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

For external use only

Do Not Use

OTC - DO NOT USE SECTION

Do not use on broken or damaged skin

When Using

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation occurs or lasts.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Directions

INDICATIONS & USAGE SECTION

apply liberally before sun exposure and as needed

children under 6 months of age: ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

dimethicone, isotridecyl isononanoate, nylon-12, diphenylsiloxy phenyl trimethicone, triethylhexanoin, synthetic wax, silica, polyethylene, sorbitan, sequilsostearate, aluminum hydroxide dimethicone/vinyldimethicone crosspolymer, euphorbia cerifera (candelilla) wax, stearic acid, diisostearyl malate, sucrose tetrastearate, triacetate, glyceryl dissostearate, pelagonium graveolens oil, tocopherol, water, butylene glycol, hydrolyzed rice bran extrace, prunus mume fruit extract, prunus yedoensis leaf extract, oryza sativa (rice) extract

Questions

OTC - QUESTIONS SECTION

Questions or Comments: Call Us 626-872-0164

PDP Image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79066-000179066-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
DIMETHICONE92RU3N3Y1OIACT
WATER059QF0KO0RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
c5785f35-6213-acdf-e053-2a95a90aba4fa7d58639-34c7-51fa-e053-2995a90a6a722021-06-23WarningsExact identifier
spl set id: a7d58639-34c7-51fa-e053-2995a90a6a72

Reported adverse events (FAERS/openFDA)#

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