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Manufacturer
Shanghai Kejing Cleaning Products Co., Ltd.
Effective date
2016-06-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:24

Label at a glance#

ProductOCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE
Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE
Label structure10 sections

Storage and handling

Other information Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Octinoxate 7.5%, Octisalate 2.0%, Oxybenzone 4.0%,

Titanium Dioxide 2.5%

OTC - PURPOSE SECTION

Purpose

Sunscreen

INDICATIONS & USAGE SECTION

Uses: Helps prevent sunburn

WARNINGS SECTION

WARNINGS:

Skin Cancer/Skin Aging Alert: Spending time in the sun

increase your risk of skin cancer and early skin aging.

this product had been shown only to prevent sunburn,

not skin cancer or skin aging.

For external use only.

Do not use on damaged or broken skin.

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

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product swallowed, get

medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply generously & evenly before sun exposure. Reapply as

needed or after towel drying, swimming or sweating.

Ask doctor before using on children under 6 months.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Cetearyl Alcohol, Xanthan Gum,

C12-15 Alkyl Benzoate, Myristyl Propionate, Propylene Glycol,

Glyceryl Stearate Citrate, Disodium EDTA, Iodopropynyl

Butylcarbamate, DMDM Hydantoin, Fragrance

STORAGE AND HANDLING SECTION

Other information

Protect this product from excessive heat and direct sun

OTC - QUESTIONS SECTION

Questions or Comment? Call toll free 1-877-254-2281

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
31190-220-302020-01-31C16284748780-19d75b9d0-159d-f424-e053-dadaa90a57cefc9282f3-3960-45b5-9d3d-39c5f3bb9a04

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
31190-220-3015 g in 1 BOTTLELOTION151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
31190-220(OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [SHANGHAI KEJING CLEANING PRODUCTS CO., LTD.]11 package rows20160627_fc9282f3-3960-45b5-9d3d-39c5f3bb9a04.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
31190-22031190-220-30

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 · Source PDF

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
412aa45f-ae59-40c2-886b-b6475899a70dfc9282f3-3960-45b5-9d3d-39c5f3bb9a042016-06-25WarningsExact identifier
spl id: 412aa45f-ae59-40c2-886b-b6475899a70d
spl set id: fc9282f3-3960-45b5-9d3d-39c5f3bb9a04

Reported adverse events (FAERS/openFDA)#

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