CH6 Color Change Black Aloforthya

Manufacturer
Rea Company | YEGREENA CO., LTD.
Effective date
2022-09-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:54:18

Label at a glance#

ProductCH6 Color Change Black Aloforthya
Active ingredientPanthenol, Salicylic Acid, Niacinamide
Label structure10 sections

Dosage and administration

■ Wet your hair sufficiently with lukewarm water, then take an appropriate amount and lather, gently massage the scalp and hair, and rinse thoroughly, ensure you’re squeaky clean.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

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 CHILDREN

Directions

DOSAGE & ADMINISTRATION SECTION

■ Wet your hair sufficiently with lukewarm water, then take an appropriate amount and lather, gently massage the scalp and hair, and rinse thoroughly, ensure you’re squeaky clean.

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 C14-16 Olefin Sulfonate, Disodium Laureth Sulfosuccinate, Lauryl Betaine, Cocamide MIPA, Lauryl Hydroxysultaine, Lauryl Glucoside, Glycerin, Fragrance, Sodium Chloride, Decyl Glucoside, Sodium Benzoate, Dipropylene Glycol, Coco-glucoside, Disodium EDTA, Polyquaternium-10, Basic Blue 99, Basic Brown 16, Tannic Acid, Guar Hydroxypropyltrimonium Chloride, Basic Yellow 87, Sodium Lauroyl Methylaminopropionate, Basic Red 51, Forsythia Suspensa Fruit Extract, Epigallocatechin Gallate, Caffeine, Biotin, Acorus Calamus Root Extract, Saccharomyces Cerevisiae Extract, Porphyra Yezoensis Extract, Butylene Glycol, Sesamum Indicum (Sesame) Seed Extract, Glycine Soja (Soybean) Seed Extract, 1,2-Hexanediol, Vitis Vinifera (Grape) Fruit Extract, Rubus Coreanus Fruit Extract, Prunus Salicina Fruit Extract, Oryza Sativa (Rice) Extract, Morus Nigra Fruit Extract, Acanthopanax Senticosus (Eleuthero) Root Extract, Hydrolyzed Soy Protein, Hydrolyzed Keratin, Hydrolyzed Elastin, Hydrolyzed Collagen, Hydrolyzed Rice Protein, Silkworm Cocoon Extract, Milk Protein Extract, Hydrolyzed Wheat Protein, Hydrolyzed Silk, Hibiscus Sabdariffa Flower Extract, Cornus Officinalis Fruit Extract, Aspalathus Linearis Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Quillaja Saponaria Bark Extract, Olea Europaea (Olive) Fruit Extract, Citrus Junos Fruit Extract, Silk Powder, Keratin Amino Acids, Ethylhexylglycerin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82916-020-022024-01-31C16284748780-10191ceaa-6a68-198a-e063-dbdaa90aec3e1ff5bb86-8841-449e-a611-6e78a2380127
82916-020-022023-07-28C16284748780-10191ceaa-6a68-198a-e063-dbdaa90aec3e1ff5bb86-8841-449e-a611-6e78a2380127

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
82916-02082916-020-01, 82916-020-02

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
1034311e-54c2-f3ad-e063-6394a90ac2061ff5bb86-8841-449e-a611-6e78a23801272024-01-30WarningsExact identifier
spl set id: 1ff5bb86-8841-449e-a611-6e78a2380127

Reported adverse events (FAERS/openFDA)#

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