SUN SCREENLOTION SPF30

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
22
Source
full-release
Hydrated at
2026-05-31 23:57:04

Label at a glance#

ProductSUN SCREENLOTION SPF30 01
Active ingredientOCTINOXATE, OXYBENZONE, AVOBENZONE
Label structure12 sections

Dosage and administration

Apply liberaaly 15 minutes before sun exposure. Children under 6 months; Ask a doctor. When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin. Do not store above 105F. May discolor some fabrics. Harmful to wood finishes and plastics.

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 liberaaly 15 minutes before sun exposure.

Children under 6 months; Ask a doctor.

OTC - DO NOT USE SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest.

Avoid contact with broken skin.

Other information

CLEANING, DISINFECTING, AND STERILIZATION INSTRUCTIONS

Do not store above 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes,Rinse with water to remove.

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 danaged or broken skin.

Other information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.

For sunscreen use

Apply to all skin exposed to the sun

Limit time in the sun,especially from 10 a.m.-2 p.m.

Wear long-s;eeved shirts,pants,hats,and sunglasses.

Warnings

WARNINGS SECTION

For external use only

DOSAGE & ADMINISTRATION SECTION

Emulsion,Apply generously 15 minutes before sun exposure

Reapply at least every 2 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackagingPackaging

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-417-01SUN SCREENLOTION SPF300145 mL in 1 BOTTLE, PLASTICLOTION4522

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-417SUN SCREENLOTION SPF30 01 (OCTINOXATE,AVOBENZONE,OXYBENZONE,TITANIUM DIOXIDE) LOTION [SHENZHEN LANTERN SCICENCE CO.,LTD.]221 package rows20231021_080c7e4f-b972-dfef-e063-6394a90a8c81.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54860-41754860-417-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
080c8f40-3c21-3cae-e063-6394a90a6ac6080c7e4f-b972-dfef-e063-6394a90a8c812023-10-18WarningsExact identifier
spl id: 080c8f40-3c21-3cae-e063-6394a90a6ac6
spl set id: 080c7e4f-b972-dfef-e063-6394a90a8c81

Reported adverse events (FAERS/openFDA)#

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