F X Fantacell Ampoule

Manufacturer
GLHKOREA
Effective date
2016-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:57

Label at a glance#

ProductF X Fantacell Ampoule
Active ingredientWitch Hazel
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Hamamelis Virginiana (Witch Hazel) Leaf Extract 0.01%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Pinus Sylvestris Leaf Extract, Fucoxanthin, Alcohol, Glycerin, Repagermanium, Hypsizygus Marmoreus Extract, Loess Extract, Pinus Densiflora Leaf Extract, Undaria Pinnatifida Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Houttuynia Cordata Extract, Angelica Gigas Root Extract, Cnidium Officinale Root Extract, Atractyloides Japonica Rhizome Extract, Sodium Hyaluronate, Adenosine, Mineral Water, Boswellia Carterii Resin Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Aloe Ferox Leaf Extract, Beta-glucan, Morus Alba Bark Extract, Glycine Soja (Soybean) Germ Extract, Caviar Extract, Vitis Vinifera (Grape) Fruit Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Pyrus Pyrifolia (Pear) Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Portulaca Oleracea Extract, Acorus Calamus Root Extract, Lavandula Angustifolia (Lavender) Extract, Cucumis Sativus (Cucumber) Fruit Extract, Arctium Lappa Root Extract, Camellia Sinensis Leaf Extract, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Triethanolamine, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. While in use of cosmetics if there is any abnomality like the following you should stop using it. If it is used continuously the symptom would be worse. So, you shall consult a dermatologist. (1) If there are any abnormalities such as redness, swelling, itching, and irritation while using (2) In the case such that the application site would have any abnormality like the above due to the direct sunlight. 2. Please do not use in areas with abnormalities such as wounds, eczema and dermatitis. 3. Storage and Handling Precautions (1) After use. the cap must be closed. two will batdeusi cap. (2) Keep out of the reach of infants and children. (3) Please do not store in the places that are hot or cold and under the direct sunlight.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of infants and children.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & usage: 1. Please spray an F-X Fantacell Solution Ampoule by using the exclusive spray device (Airbrush Compressor) 2. Fill an Airbrush with a half bottle of an F-X Fantacell Solution Ampoule each time and spray it directly to the body parts such as face, neck, hands, feet, full body and etc.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: The amount to use is recommended to be once per two days. Or you may add or reduce some of the amount to use depending on skin conditions. (1) After clearing makeup and washing the face, please gently spray in the face. (2) You may use it gently spraying in the face in a state with makeup. (3) It would be better if the ampoule is used after cleansing the face before bed. (4) It would take 5~10 minutes to spray a half bottle of the ampoule on the face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809366000783GTIN-13: 8809366000783
EAN-13: 8809366000783
GTIN storage (14 digits): 08809366000783
f x fantacell solution ampoule carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71081-010-022020-01-31C16284748780-19d75b9d0-097f-f424-e053-dadaa90a57cef5de7c83-ea46-48f6-bffc-e6519edbda9f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71081-010-01F X Fantacell Ampoule8 mL in 1 VIALSOLUTION81
71081-010-02F X Fantacell Ampoule16 in 1 CARTONSOLUTION161

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71081-010F X FANTACELL AMPOULE (WITCH HAZEL) SOLUTION [GLHKOREA]1Legacy NDC, 2 package rows20161109_f5de7c83-ea46-48f6-bffc-e6519edbda9f.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
71081-01071081-010-01, 71081-010-02

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
Witch Hazel101I4J0U34ACTIB
Water059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT

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
8075776d-64d4-4fd6-949f-d190e4230e15f5de7c83-ea46-48f6-bffc-e6519edbda9f2016-11-09WarningsExact identifier
spl id: 8075776d-64d4-4fd6-949f-d190e4230e15
spl set id: f5de7c83-ea46-48f6-bffc-e6519edbda9f

Reported adverse events (FAERS/openFDA)#

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