CH6 Perfumed Aloforthya Aromatic herb

Manufacturer
Rea Company | YEGREENA CO., LTD.
Effective date
2022-09-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:53:15

Label at a glance#

ProductCH6 Perfumed Aloforthya Aromatic herb
Active ingredientDEXPANTHENOL, SALICYLIC ACID, NIACINAMIDE
Label structure10 sections

Dosage and administration

■ Soak your hair in lukewarm water, then squeeze out the proper amount of foam and gently massage your scalp and hair before rinsing .

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

D-Panthenol 0.2%
Salicylic Acid 0.2%
Niacinamide 0.1%

PURPOSE

OTC - PURPOSE SECTION

Anti-hair loss

Use(s)

INDICATIONS & USAGE SECTION

■ To recover the scalp condition for healthier.
■ To strengthen hair root, give growth stimulation and thicken hair

Warnings

WARNINGS SECTION

1. If there are troubles such as red spot, swelling or itching on the region used or concerns about side effect in using cosmetics or by direct sunlight consult a specialist.
2. Refrain from using the product on the wounded area.
3. Instructions for storage and handling A) Keep out of the reach of children.
B) Keep away from direct sunlight.
4. In case of eyes contact, immediately wash out.
5. Take precautions because if you do not rinse it out with water after using it as it may cause hair loss or discoloration.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ Keep out of reach of infants and children.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Soak your hair in lukewarm water, then squeeze out the proper amount of foam and gently massage your scalp and hair before rinsing .

Other Information

OTHER SAFETY INFORMATION

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

Questions

OTC - QUESTIONS SECTION

■ +82-2-2257-8882
■ ch6mall.com

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Glycerin, Sodium Citrate, Sodium Benzoate, PPG-3 Caprylyl Ether, Sodium Chloride, Decyl Glucoside, TEA-Cocoyl Glutamate, Coco-glucoside, Forsythia Suspensa Fruit Extract, Dipropylene Glycol, Echinacea Angustifolia Root Extract, Yucca Schidigera Root Extract, Saponaria Officinalis Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Quillaja Saponaria Bark Extract, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Citrus Junos Fruit Extract, Sophora Angustifolia Root Extract, Butylene Glycol, 1,2-Hexanediol, Hibiscus Sabdariffa Flower Extract, Cornus Officinalis Fruit Extract, Aspalathus Linearis Extract, Cetrimonium Chloride, Steartrimonium chloride, Propylene glycol, Ethylhexylglycerin, Rice sh-Oligopeptide-1, Hydrogenated Lecithin, Simmondsia Chinensis (Jojoba) Seed Oil, Ricinus Communis (Castor) Seed Oil, Macadamia Ternifolia Seed Oil, Glyceryl Citrate/Lactate/Linoleate/Oleate, Glyceryl Oleate, Glycolipids, Tocopherol, Ceramide NP, Glycosphingolipids, Guar Hydroxypropyltrimonium Chloride, Polyquaternium-10, Disodium EDTA, Polyquaternium-7, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82916-080-022024-01-31C16284748780-10191ceaa-7213-198a-e063-dbdaa90aec3e0694c046-d386-4071-a1cd-0ea81dd9edc4
82916-080-022023-07-28C16284748780-10191ceaa-7213-198a-e063-dbdaa90aec3e0694c046-d386-4071-a1cd-0ea81dd9edc4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82916-08082916-080-01, 82916-080-02

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
10344cbc-3a1c-95e8-e063-6294a90a0cbb0694c046-d386-4071-a1cd-0ea81dd9edc42024-01-30WarningsExact identifier
spl set id: 0694c046-d386-4071-a1cd-0ea81dd9edc4

Reported adverse events (FAERS/openFDA)#

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