FDA.reportPublic FDA data

Sun Block

Manufacturer
Yuyao Jessie Promotional Products Co., Ltd.
Effective date
2010-07-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:25:05

Label at a glance#

ProductSun Block
Active ingredientOCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, HOMOSALATE
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

OctylMethoxycinnamate,Benzophenone-3,Homosalate, Titanium dioxide

Use

INDICATIONS & USAGE SECTION

Protection from the sun’s damaging effects

Warnings

WARNINGS SECTION

For external use only                                                         
Not recommended for children under 6 months of age

Direction

DOSAGE & ADMINISTRATION SECTION

Apply liberally and evenly before sun exposure.   

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water,CetearylAlcohol,Glycerinmonostearate,                               
Gctt,Propylparaben,Methylparaben,                                    
glycerol,EDTA-2NA,Vinylchloride-methylacrylate,                   
copolymer,Methylisothiazolinone 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label of sunscreen
label of sunscreen

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51414-200-012019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-022019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-032019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-042019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-052019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-062019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-072019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-082019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-092019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-102019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-112019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-122019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-132019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-142019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT
51414-200-152019-10-21C16284748780-1956f9ecf-d43a-621f-e053-dbdaa90a74adSunblock DRUG FACT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51414-200-01Sun Block15 mL in 1 BOTTLECREAM152
51414-200-02Sun Block20 mL in 1 BOTTLECREAM202
51414-200-03Sun Block30 mL in 1 BOTTLECREAM302
51414-200-04Sun Block40 mL in 1 BOTTLECREAM402
51414-200-05Sun Block50 mL in 1 BOTTLECREAM502
51414-200-06Sun Block60 mL in 1 BOTTLECREAM602
51414-200-07Sun Block70 mL in 1 BOTTLECREAM702
51414-200-08Sun Block80 mL in 1 BOTTLECREAM802
51414-200-09Sun Block90 mL in 1 BOTTLECREAM902
51414-200-10Sun Block100 mL in 1 BOTTLECREAM1002
51414-200-11Sun Block200 mL in 1 BOTTLECREAM2002
51414-200-12Sun Block250 mL in 1 BOTTLECREAM2502
51414-200-13Sun Block300 mL in 1 BOTTLECREAM3002
51414-200-14Sun Block400 mL in 1 BOTTLECREAM4002
51414-200-15Sun Block500 mL in 1 BOTTLECREAM5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51414-200SUN BLOCK (OCTYL METHOXYCINNAMATE BENZOPHENONE-3 TITANIUM DIOXIDE HOMOSALATE) CREAM [YUYAO JESSIE PROMOTIONAL PRODUCTS CO., LTD.]2Legacy NDC, 15 package rows20100707_f9e0f06c-3c58-4070-b29b-7df35cc2aa4e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HOMOSALATEACTIVE INGREDIENTV06SV4M95S2
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y2
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
HOMOSALATEACTIVE MOIETYV06SV4M95S2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
OXYBENZONEACTIVE MOIETY95OOS7VE0Y2
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51414-20051414-200-01, 51414-200-02, 51414-200-03, 51414-200-04, 51414-200-05, 51414-200-06, 51414-200-07, 51414-200-08, 51414-200-09, 51414-200-10, 51414-200-11, 51414-200-12, 51414-200-13, 51414-200-14, 51414-200-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OXYBENZONE95OOS7VE0YACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
HOMOSALATEV06SV4M95SACTIB

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
ead90432-b6f9-457d-a022-b0c76a2e9d24f9e0f06c-3c58-4070-b29b-7df35cc2aa4e2010-07-07WarningsExact identifier
spl id: ead90432-b6f9-457d-a022-b0c76a2e9d24
spl set id: f9e0f06c-3c58-4070-b29b-7df35cc2aa4e

Reported adverse events (FAERS/openFDA)#

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