Vital Fluid II EGF and FGF Whitening Serum

Manufacturer
AMAROS CO., LTD.
Effective date
2019-04-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:59:09

Label at a glance#

ProductVital Fluid II EGF and FGF Whitening Serum
Active ingredientAllantoin
Label structure8 sections

Indications and uses

Indication and Usage: 1. Tighten the lid after using it. 2. Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.3. Use it in the morning or evening after washing face.

Dosage and administration

Dosage and Administration: Every morning and evening, apply 2-3 drops on cleaned face skin, avoiding eye area, finish with light sweeping movements. For best result, follow with the appropriate skincare cream.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Allantoin 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Butylene Glycol, Arbutin, Betaine, Polyquaternium-51, Coceth-7(and)PPG-1-PEG-9 Lauryl Glycol Ether(and)PEG-40 Hydrogenated Castor Oil, Beta-Glucan, Morus Alba Bark Extract, Camellia Sinensis Leaf Extract, Caprylyl Glycol (and) Caprylhydroxamic Acid, Acetyl Hexapeptide-8, Arginine, Carbomer, Tocopheryl Acetate, Adenosine, Disodium EDTA, Dipotassium Glycyrrhizate, Human Oligopeptide-13, Human Oligopeptide-1, Fragrance.

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. In case of having following symptoms after using this product, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: Keep out of reach of babies and children.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Indication and Usage: 1. Tighten the lid after using it. 2. Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight.3. Use it in the morning or evening after washing face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and Administration: Every morning and evening, apply 2-3 drops on cleaned face skin, avoiding eye area, finish with light sweeping movements. For best result, follow with the appropriate skincare cream.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60899-100-012022-01-28C16284748780-1d6a99b39-35d2-a426-e053-dadaa90af4c2a3868721-7531-4406-997a-eba4a4792aa0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60899-100-01Vital Fluid II EGF and FGF Whitening Serum30 mL in 1 CARTONCREAM302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60899-100VITAL FLUID II EGF AND FGF WHITENING SERUM (ALLANTOIN) CREAM [AMAROS CO., LTD.]2Legacy NDC, 1 package rows20190411_a3868721-7531-4406-997a-eba4a4792aa0.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AllantoinACTIVE INGREDIENT344S277G0Z1
ALLANTOINACTIVE MOIETY344S277G0Z1
ArbutinINACTIVE INGREDIENTC5INA23HXF1
WaterINACTIVE INGREDIENT059QF0KO0R1

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
60899-10060899-100-01

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
Allantoin344S277G0ZACTIB
Water059QF0KO0RIACT
ArbutinC5INA23HXFIACT

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
dc193cc3-07f9-4b70-89d1-3bcf3c65bdf1a3868721-7531-4406-997a-eba4a4792aa02019-04-11WarningsExact identifier
spl id: dc193cc3-07f9-4b70-89d1-3bcf3c65bdf1
spl set id: a3868721-7531-4406-997a-eba4a4792aa0

Reported adverse events (FAERS/openFDA)#

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