Dr.Double Ha ULTRA SOOTHING ESSENCE

Manufacturer
GK COSMETIC CO., LTD.
Effective date
2020-12-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:00

Label at a glance#

ProductDr.Double Ha ULTRA SOOTHING ESSENCE
Active ingredientHOUTTUYNIA CORDATA FLOWERING TOP, PERILLA FRUTESCENS LEAF
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Houttuynia Cordata Extract, Perilla Frutescens Leaf Extract

INACTIVE INGREDIENT SECTION

Acanthopanax Senticosus (Eleuthero) Root Extract, Camellia Sinensis Leaf Extract, Portulaca Oleracea Extract, Ganoderma Lucidum (Mushroom) Extract, Spirodela Polyrrhiza Extract, Picrasma Excelsa Wood Extract, Phellinus Linteus Extract, Nelumbium Speciosum Flower Extract, 1,2-Hexanediol, Butylene Glycol, Dipropylene Glycol, Zanthoxylum Piperitum Fruit Extract, Pulsatilla Koreana Extract, Usnea Barbata (Lichen) Extract, Rehmannia Glutinosa Root Extract, Schizonepeta Tenuifolia Extract, Saururus Chinensis Leaf/Root Extract, Polygonum Fagopyrum Seed Extract, Glycine Max (Soybean) Seed Extract, Ulmus Davidiana Root Extract, Poria Cocos Extract, Ginkgo Biloba Leaf Extract, Prunus Armeniaca (Apricot) Kernel Extract, Sanguisorba Officinalis Root Extract, Phellodendron Amurense Bark Extract, Prunus Mume Fruit Extract, Pinus Densiflora Extract, Magnolia Obovata Bark Extract, Polygonum Cuspidatum Root Extract, Sophora Angustifolia Root Extract, Ganoderma Lucidum (Mushroom) Stem Extract, Carthamus Tinctorius (Safflower) Flower Extract, Oryza Sativa (Rice) Bran Extract, Ethylhexylglycerin, Polyglyceryl-10 Laurate, Polyglyceryl-10 Myristate, Glycerin, Aniba Rosodora (Rosewood) Wood Oil, Allantoin, Disodium EDTA, Panthenol

OTC - PURPOSE SECTION

Skin protectant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


INDICATIONS & USAGE SECTION

Clean the skin before use, spray an appropriate amount, and massage it to absorb enough. It can be used in all skin areas including the face and scalp.

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

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70098-0017-22022-01-28C16284748780-1d6a99b39-818e-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70098-0017-2Dr.Double Ha ULTRA SOOTHING ESSENCE50 mL in 1 BOTTLE, SPRAYLIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70098-0017DR.DOUBLE HA ULTRA SOOTHING ESSENCE (HOUTTUYNIA CORDATA EXTRACT, PERILLA FRUTESCENS LEAF EXTRACT) LIQUID [GK COSMETIC CO., LTD.]1Legacy NDC, 1 package rows20201229_b77f7242-c2e1-414b-e053-2a95a90abb81.zip

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
70098-001770098-0017-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b77f7242-c2e2-414b-e053-2a95a90abb81b77f7242-c2e1-414b-e053-2a95a90abb812020-12-27WarningsExact identifier
spl id: b77f7242-c2e2-414b-e053-2a95a90abb81
spl set id: b77f7242-c2e1-414b-e053-2a95a90abb81

Reported adverse events (FAERS/openFDA)#

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