FDA.reportPublic FDA data

SunScreen Lotion SPF30

Manufacturer
Shanghai Kejing Cleaning Products Co., Ltd.
Effective date
2010-04-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:24:14

Label at a glance#

ProductSunScreen SPF30
Active ingredientHOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                                                                Purpose

Homosalate 5 percent, Octinoxate 7.5 percent,
Octisalate 5 percent, Oxybenzone 4.25 percent............................................Sunscreen

OTC - PURPOSE SECTION

Uses: Helps prevent sunburn

WARNINGS SECTION

Warnings: For external use only.

OTC - WHEN USING SECTION

When using this product:  Avoid contact with eyes, In case of eye contact, flush with plenty of water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions. Apply generously and evenly before sun exposure.
Reapply as needed or after towel drying, swimming,or sweating. Ask doctor before using on children under 6 months.

DESCRIPTION SECTION

Other information.
Sun Alert: Limiting sun exposure and using sunscreens may
reduce the risk of skin aging, skin cancer, and other harmful
effects of the sun.

SPF30 SUNSCREEN SPRAY

UVAand UVB PROTECTION

Distributed by Tekweld Inc.
180 Central Avenue,
FARMINGDALE,NY11735

made in China          MFG:90807

INACTIVE INGREDIENT SECTION

Inactive ingredients: Acrylates/Octylacrylamide copolymer,
Alcohol Denat, Dimethicone, Fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF 30

SunScreen Lotion

UVA and UVB PROTECTION

Active ingredient                                                                                Purpose

Homosalate 5 percent, Octinoxate 7.5 percent,
Octisalate 5 percent, Oxybenzone 4.25 percent ..............................Sunscreen                             
0.34 FL OZ (10 mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunScreenLotion60mlSunScreenLotion60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunScreenLotionSPFSunScreenLotionSPF

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SunScreen Lotion

SPF30

UVA and UVB

PROTECTION

EASY CONTROL SPRAY MIST

GOES ANYWHERE POCKET, PURSE, OR PACK

0.34 FL OZ (10mL)

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
31190-200-102019-10-21C16284748780-1956f9ecf-de36-621f-e053-dbdaa90a74adSunScreen Lotion SPF30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
31190-200-10SunScreen SPF301 in 1 CARTONLOTION14
31190-200-10SunScreen SPF3010 mL in 1 BOTTLE, SPRAYLOTION104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
31190-200SUNSCREEN SPF30 (HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE) LOTION [SHANGHAI KEJING CLEANING PRODUCTS CO., LTD.]4Legacy NDC, 2 package rows20100415_d928a1a5-d32a-405d-bac4-20ed54bd8a59.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HOMOSALATEACTIVE INGREDIENTV06SV4M95S4
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD514
OCTISALATEACTIVE INGREDIENT4X49Y0596W4
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y4
HOMOSALATEACTIVE MOIETYV06SV4M95S4
OCTINOXATEACTIVE MOIETY4Y5P7MUD514
OCTISALATEACTIVE MOIETY4X49Y0596W4
OXYBENZONEACTIVE MOIETY95OOS7VE0Y4
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O4

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
31190-20031190-200-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OXYBENZONE95OOS7VE0YACTIB
DIMETHICONE92RU3N3Y1OIACT

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
9be4854e-39ac-45ca-91d6-d01576baa281d928a1a5-d32a-405d-bac4-20ed54bd8a592010-04-15WarningsExact identifier
spl id: 9be4854e-39ac-45ca-91d6-d01576baa281
spl set id: d928a1a5-d32a-405d-bac4-20ed54bd8a59

Reported adverse events (FAERS/openFDA)#

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