MOISTURIZE AND COOLSUNSCREEN LOTION SPF50

Manufacturer
Shenzhen Lantern Scicence Co.,Ltd. | LANTERN HEALTH&BEAUTY LAB INC. | Shenzhen Lantern Science Co.,Ltd.
Effective date
2023-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:56:59

Label at a glance#

ProductLANTERN SUNSCREEN SPF50 01
Active ingredientTITANIUM DIOXIDE, AVOBENZONE, OCTINOXATE
Label structure13 sections

Dosage and administration

Apply liberally 15 minutes before sunexposure. Use a water resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a docto

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHYLHEXYL METHOXYCINNAMATE:8.5%

Avobenzone:3.0%

Titanium dioxide:3.0% Sunscreen

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA, METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHE NOL, AQUA, DECYL GLUCOSIDE, PROPYLENE GLYCOL, XANTHAN GUM, GLYCERIN, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, ETHYLHEXYL TRIAZONE, DIMETHICONE, PEG-20 METHYL GLUCOSE SESQUISTEARATE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, METHYL GLUCOSE SESQUISTEARATE, PHENOXYETHANOL, TOCOPHERYL ACETATE, PARFUM, MENTHOL, METHYLPARABEN, BISABOLOL, ALLANTOIN, PROPYLPARABEN, DISODIUM EDTA, SPIRULINA PLATENSIS EXTRACT, SODIUM HYALURONATE.

Directions

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before sunexposure.
Use a water resistant sunscreen if swimming or sweating.
Reapply at least every 2 hours.
Children under 6 months: Ask a docto

When using this product

OTC - WHEN USING SECTION

Keep out of reach of children.
If product is swallowed, get medical help or contact a Poison Control Center rightaway

Purpose

OTC - PURPOSE SECTION

Sunscreen

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs.

Do not use

OTC - DO NOT USE SECTION

On damaged or broken skin.
When using this product keep out of eyes.
Rinse with water to remove

Other information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sunlight

warnings

WARNINGS SECTION

For external use only.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Dosage & administration section

Apply liberally 15 minutes before sunexposure.
Use a water resistant sunscreen if swimming or sweating.
Reapply at least every 2 hours.
Children under 6 months: Ask a docto

package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackaging

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-416-01LANTERN SUNSCREEN SPF500145 g in 1 TUBEPASTE453

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-416LANTERN SUNSCREEN SPF50 01 (LANTERN) PASTE [SHENZHEN LANTERN SCICENCE CO.,LTD.]31 package rows20231020_07f90e7f-9c9e-e139-e063-6394a90ad8ef.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54860-41654860-416-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
07f8f075-b31a-bcc0-e063-6394a90af7f207f90e7f-9c9e-e139-e063-6394a90ad8ef2023-10-18WarningsExact identifier
spl id: 07f8f075-b31a-bcc0-e063-6394a90af7f2
spl set id: 07f90e7f-9c9e-e139-e063-6394a90ad8ef

Reported adverse events (FAERS/openFDA)#

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