MediSpa Sunblock

Manufacturer
Universal Cosmetic Co., Ltd
Effective date
2010-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:27

Label at a glance#

ProductMediSpa Sunblock sunblock
Active ingredientZINC OXIDE, OCTINOXATE, ENZACAMENE, AVOBENZONE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl Methoxycinnamate, Zinc Oxide, 4-Methylbenzylidene camphor, Butyl Mehoxydibenzoylmethane

DESCRIPTION SECTION

Uses
■ Perfectly blocks both UVA and UVB rays without stimuli
■ Provides high protection from sunburn
■ Suitable for skin that underwent medical treatment

Warning
For external use only
When using this product
■    Avoid eye area. If contact occurs, rinse eyes thoroughly
■  Discontinue use if signs of irritation develops
Keep out of reach of the children

Direction
■ Rub a proper quantity over the whole face, before finishing skincare.

Other Information
■ store between 20-25 °C (68-77 °F)
■ avoid freezing and excessive heat above 40 °C (104 °F)
■ close cap after use.

Inactive Ingredient
■ Water ■ Cyclomethicone ■ Dimethicone/Vinyl Dimethicone Crosspolymer ■ C12-15 Alkyl Benzoate ■ Glycerin ■ Cetyl PEG/PPG-10/1 Dimethicone ■ Beeswax ■ Sodium Chloride ■ Sorbitan Sesquiolate ■ C20-40 acid ■ Methylparaben ■ Polyethylene ■ Brassica Campestris Sterols ■ Propylparaben ■ Disodium EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

box label
box label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52554-1001-12019-10-21C16284748780-1956f9ecf-cf06-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52554-1001-1MediSpa Sunblocksunblock70 mL in 1 BOTTLE, WITH APPLICATORCREAM701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52554-1001MEDISPA SUNBLOCK SUNBLOCK (ZINC OXIDE) CREAM [UNIVERSAL COSMETIC CO., LTD]1Legacy NDC, 1 package rows20100806_2eda1a2b-e024-449b-9553-839cdad9aab3.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
ENZACAMENEACTIVE INGREDIENT8I3XWY40L91
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
ENZACAMENEACTIVE MOIETY8I3XWY40L91
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52554-100152554-1001-1

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
ZINC OXIDESOI2LOH54ZACTIB
OCTINOXATE4Y5P7MUD51ACTIB
ENZACAMENE8I3XWY40L9ACTIB
AVOBENZONEG63QQF2NOXACTIB

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
ad7e144f-288c-4513-86f1-c9d82bd803592eda1a2b-e024-449b-9553-839cdad9aab32010-08-04Exact identifier
spl id: ad7e144f-288c-4513-86f1-c9d82bd80359
spl set id: 2eda1a2b-e024-449b-9553-839cdad9aab3

Reported adverse events (FAERS/openFDA)#

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