LUMINANT UMBRELLA MASK PACK

Manufacturer
GK COSMETIC CO., LTD.
Effective date
2019-12-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:01:45

Label at a glance#

ProductLUMINANT UMBRELLA MASK PACK
Active ingredientALLANTOIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

allantoin


INACTIVE INGREDIENT SECTION

glycerin, butylene glycol, etc.


OTC - PURPOSE SECTION

skin protectant


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


INDICATIONS & USAGE SECTION

1. After wash your face, take our STEP01 Luminant Umbrella Facial Mask and put it on your face.

2. Take off the sheet after 15 to 20 minutes when it gets absorbed into your skin

3. Tap your skin softly for your skin to absorb anything left on the skin.

4. Put STEP02 Luminant Whitening Aqua Creme(2 ml) evenly on your face.

When we consider skin turn over period, using the productconsistently for

4 weeks is the most effective way to use the product.

WARNINGS SECTION

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70098-0002-12022-01-28C16284748780-1d6a99b39-8587-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70098-0002-1LUMINANT UMBRELLA MASK PACK38 mL in 1 PACKAGELIQUID382

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70098-0002LUMINANT UMBRELLA MASK PACK (ALLANTOIN) LIQUID [GK COSMETIC CO., LTD.]2Legacy NDC, 1 package rows20191206_10432ad6-1fc4-489a-8510-f338443035fd.zip

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
70098-000270098-0002-1

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
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZACTIB

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
9903c86d-e1fd-24aa-e053-2a95a90adca610432ad6-1fc4-489a-8510-f338443035fd2019-12-06WarningsExact identifier
spl id: 9903c86d-e1fd-24aa-e053-2a95a90adca6
spl set id: 10432ad6-1fc4-489a-8510-f338443035fd

Reported adverse events (FAERS/openFDA)#

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