87911-001-002-003 Luxe Gloss Hydrating Lip Gloss SPF 35

Manufacturer
Lale Cosmetics LLC | Foshan Sugar Max Cosmetics CO.,Ltd
Effective date
2026-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-05 06:00:06

Label at a glance#

ProductLuxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY
Active ingredientOCTOCRYLENE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 8%
Octisalate 5%
Titanium Dioxide 6%
Zinc Oxide 8%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

helps prevent sunbum.

if used as directed with other sun protection measures (seeDirections), decreases the risk ofskin cancer and early skin agingcaused by the sun.

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

DOSAGE & ADMINISTRATION SECTION

apply liberally 15 minutes before sun exposure.
reapply at least every 2 hours or after eating, drinking, or sun exposure.

INACTIVE INGREDIENT SECTION


Hydrogenated Polyisobutene,
Polybutene, C12-15 Alkyl
Benzoate, Microcrystalline Wax,
Acrylates/Octylacrylamide
Copolymer, Trimethylsiloxysilicate,
Silica Dimethyl Silylate, CI 77491,
CI15850, CI77492, CI77499,
Tocopherol, Bisabolol, Fragrance,
Aluminum Hydroxide,
Triethoxycaprylylsilane

INACTIVE INGREDIENT SECTION


Hydrogenated Polyisobutene,
Polybutene, C12-15 Alkyl
Benzoate, Microcrystalline
Wax, Acrylates/Octylacrylamide
Copolymer, Trimethylsiloxysili-
cate, Silica Dimethyl Silylate,
Tridecyl Trimellitate, CI 16035,
Tocopherol, CI 15850,
Bisabolol, Fragrance, CI 77499,
CI77491,CI77492

INACTIVE INGREDIENT SECTION


Hydrogenated Polyisobutene,
Polybutene, C12-15 Alkyl
Benzoate, Microcrystalline Wax,
Acrylates/Octylacrylamide
Copolymer, Trimethylsiloxysilicate,
Silica Dimethyl Silylate, CI 77491,
CI 15850, CI 77492, Tocopherol,
Bisabolol, Fragrance, CI 15985,
Aluminum Hydroxide,
Triethoxycaprylylsilane, Mica

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130860015898111GTIN-13: 0860015898111
EAN-13: 0860015898111
GTIN-12: 860015898111
UPC-A: 860015898111
GTIN storage (14 digits): 00860015898111
label2.jpg
BarcodeEAN-130860015898128GTIN-13: 0860015898128
EAN-13: 0860015898128
GTIN-12: 860015898128
UPC-A: 860015898128
GTIN storage (14 digits): 00860015898128
label3.jpg
BarcodeEAN-130860015898135GTIN-13: 0860015898135
EAN-13: 0860015898135
GTIN-12: 860015898135
UPC-A: 860015898135
GTIN storage (14 digits): 00860015898135
label1.jpg

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87911-00187911-001-01
87911-00287911-002-01
87911-00387911-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 58 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEYOCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8%Lale Cosmetics LLC581fb0cd-c55d-d562-e063-6394a90a7f112026-08-03WarningsExact identifier
ndc (package): 87911-003-01
ndc (package): 87911-001-01
ndc (package): 87911-002-01
ndc (product): 87911-003
ndc (product): 87911-001
ndc (product): 87911-002
ndc11 (package): 87911000101
ndc11 (package): 87911000301
ndc11 (package): 87911000201
spl id: 581fb0cd-c55e-d562-e063-6394a90a7f11
spl set id: 581fb0cd-c55d-d562-e063-6394a90a7f11

Reported adverse events (FAERS/openFDA)#

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