Laser Block 100

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 22:25:28

Label at a glance#

ProductLaser Block 100 sunblock
Active ingredientOCTINOXATE, ZINC OXIDE, ENZACAMENE, TITANIUM DIOXIDE, AMILOXATE, AVOBENZONE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethylhexyl Methoxycinnamate, Zinc Oxide,  4-Methylbenzylidene camphor, Titanium Dioxide, Isoamyl p-Methoxycinnamate, Butyl Methoxydibenzoylmethane

DESCRIPTION SECTION

Uses
■ Perfectly blocks UV rays without stimuli
■ Effective against
l    PIH(Post Inflammatory Pigmentation)
l    Photosensitive skins
l    DNA destruction
■ Suitable for skin that underwent medical treatment
■ Helps keep moisturize


Warning
For external use only
When using this product
■    Avoid eye area. If contact occurs, rinse eyes thoroughly
■  If following abnormal symptoms occurs after use, stop use and ask doctor
l    red specks, swelling, itching
Keep out of reach of the children

    
Direction
■ Before finishing skincare, rub a proper quantity over the whole face that underwent IPL or Laser therapy.

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
52554-3001-12019-10-21C16284748780-1956f9ecf-db87-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52554-3001-1Laser Block 100sunblock50 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52554-3001LASER BLOCK 100 SUNBLOCK (OCTINOXATE) CREAM [UNIVERSAL COSMETIC CO., LTD]1Legacy NDC, 1 package rows20100806_b81b277d-de03-4130-812b-37ef5d54feb2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMILOXATEACTIVE INGREDIENT376KTP06K81
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
ENZACAMENEACTIVE INGREDIENT8I3XWY40L91
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
AMILOXATEACTIVE MOIETY376KTP06K81
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
ENZACAMENEACTIVE MOIETY8I3XWY40L91
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

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
52554-300152554-3001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
eed3377a-26c2-4e93-95c4-7f10712d90beb81b277d-de03-4130-812b-37ef5d54feb22010-08-04Exact identifier
spl id: eed3377a-26c2-4e93-95c4-7f10712d90be
spl set id: b81b277d-de03-4130-812b-37ef5d54feb2

Reported adverse events (FAERS/openFDA)#

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