MediSpa SunSpray

Manufacturer
Universal Cosmetic Co., Ltd
Effective date
2010-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:27

Label at a glance#

ProductMediSpa SunSpray sunblock
Active ingredientOCTINOXATE, ENZACAMENE, OCTOCRYLENE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl Methoxycinnamate, 4-Methylbenzylidene camphor, Octocrylene

DESCRIPTION SECTION

 Uses
■ Helps prevent sunburn
■ Provides high protection from sunburn
■ Helps keep moisturize
■ Can be sprayed on powdered face

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
■ Spray 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52554-2001-12019-10-21C16284748780-1956f9ecf-d9b9-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52554-2001-1MediSpa SunSpraysunblock55 mL in 1 BOTTLE, WITH APPLICATORSPRAY551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52554-2001MEDISPA SUNSPRAY SUNBLOCK (OCTINOXATE) SPRAY [UNIVERSAL COSMETIC CO., LTD]1Legacy NDC, 1 package rows20100806_340929aa-6fd8-49e9-932e-b4851caa0b02.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ENZACAMENEACTIVE INGREDIENT8I3XWY40L91
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTOCRYLENEACTIVE INGREDIENT5A68WGF6WM1
ENZACAMENEACTIVE MOIETY8I3XWY40L91
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTOCRYLENEACTIVE MOIETY5A68WGF6WM1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52554-200152554-2001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
ENZACAMENE8I3XWY40L9ACTIB
OCTOCRYLENE5A68WGF6WMACTIB

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
7dd4f01c-7789-46a4-8617-c0782e79ccdf340929aa-6fd8-49e9-932e-b4851caa0b022010-08-06Exact identifier
spl id: 7dd4f01c-7789-46a4-8617-c0782e79ccdf
spl set id: 340929aa-6fd8-49e9-932e-b4851caa0b02

Reported adverse events (FAERS/openFDA)#

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