SPF 30 SUNSCREEN

Manufacturer: Shanghai Kejing Cleaning Products Co., Ltd.
Effective date: 2016-07-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:46:34

Label at a glance#

ProductSPF 30 SUNSCREEN

Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE

Label structure10 sections

Storage and handling

Other information Protect this product from excessive heat and direct sun

Contacts and useful links#

PhoneLabel contact1-877-254-2281

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 description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
31190-320-30	2020-01-31	C162847	48780-1	9d75b9cf-f47f-f424-e053-dadaa90a57ce	eac95a67-c877-443b-8e96-537f92c5c9cf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
31190-320-30	SPF 30 SUNSCREEN	15 g in 1 BOTTLE	LOTION	15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
31190-320	SPF 30 SUNSCREEN (OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [SHANGHAI KEJING CLEANING PRODUCTS CO., LTD.]	1	Legacy NDC, 1 package rows	20160718_eac95a67-c877-443b-8e96-537f92c5c9cf.zip

Products#

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

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

SPF 30 SUNSCREEN
OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE
OCTINOXATE
OCTISALATE
OXYBENZONE
TITANIUM DIOXIDE
WATER
CETOSTEARYL ALCOHOL
XANTHAN GUM
ALKYL (C12-15) BENZOATE
MYRISTYL PROPIONATE
PROPYLENE GLYCOL
GLYCERYL STEARATE CITRATE
EDETATE DISODIUM
IODOPROPYNYL BUTYLCARBAMATE
DMDM HYDANTOIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
31190-320	31190-320-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
OXYBENZONE	95OOS7VE0Y	ACTIB
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
WATER	059QF0KO0R	IACT
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
XANTHAN GUM	TTV12P4NEE	IACT
ALKYL (C12-15) BENZOATE	A9EJ3J61HQ	IACT
MYRISTYL PROPIONATE	P59053E7NJ	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
GLYCERYL STEARATE CITRATE	WH8T92A065	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
IODOPROPYNYL BUTYLCARBAMATE	603P14DHEB	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6fc072cf-c5bc-434a-bd0d-899925cd489d			eac95a67-c877-443b-8e96-537f92c5c9cf	2016-07-17	Warnings	Exact identifier spl id: 6fc072cf-c5bc-434a-bd0d-899925cd489d spl set id: eac95a67-c877-443b-8e96-537f92c5c9cf

Reported adverse events (FAERS/openFDA)#

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