QUIKSILVER SPF 30 SUNSCREEN

Manufacturer
Shenzhen Lantern Scicence Co.,Ltd. | LANTERN HEALTH&BEAUTY LAB INC. | Shenzhen Lantern Science Co.,Ltd. | Greater Pacific Industries,Inc.
Effective date
2021-09-17
Label type
HUMAN OTC DRUG LABEL
Version
21
Source
full-release
Hydrated at
2026-05-31 23:42:26

Label at a glance#

ProductQUIKSILVER SPF 30 SUNSCREEN 01
Active ingredientHOMOSALATE, AVOBENZONE, OCTINOXATE, OCTOCRYLENE
Label structure10 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#

Drug Facts

DESCRIPTION SECTION

54860-382-01.54860-382-01.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Avobenzone 1.0%

Ethylhexyl Methoxycinnamate 8.0%

Homosalate 2.0%

Octocrylene 2.0% ..........................................Sunscreen

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA,CYCLOPENTASILOXANE,ISOHEXADECANE,ETHYLHEXYL METHOXYCINNAMATE,GLYCERIN,BUTYLENE GLYCOL,CETYL PEG/PPG-10/1 DIMETHICONE,HOMOSALATE,OCTOCRYLENE,SODIUM CHLORIDE,AVOBENZONE,POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE,DISTEARDIMONIUM HECTORITE,PHENOXYETHANOL,HYDROXYACETOPHENONE,PARFUM,BISABOLOL,DISODIUM EDTA.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54860-382-0154860-382-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-383-012022-07-29C16284748780-1e4f33bdf-a6e1-d8a0-e053-dadaa90a6e4eQUIKSILVER SPF 30 SUNSCREEN

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-383-01QUIKSILVER SPF 30 SUNSCREEN0130 g in 1 BOTTLE, PLASTICLOTION3021

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-383QUIKSILVER SPF 30 SUNSCREEN 01 (AVOBENZONE,ETHYLHEXYL METHOXYCINNAMATE,HOMOSALATE,OCTOCRYLENE) LOTION [SHENZHEN LANTERN SCICENCE CO.,LTD.]21Legacy NDC, 1 package rows20210919_cbebe020-f475-7f61-e053-2995a90a8972.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54860-38354860-383-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
cc3c3b32-2671-604b-e053-2995a90a71f8cbebe020-f475-7f61-e053-2995a90a89722021-09-17Exact identifier
spl id: cc3c3b32-2671-604b-e053-2995a90a71f8
spl set id: cbebe020-f475-7f61-e053-2995a90a8972

Reported adverse events (FAERS/openFDA)#

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