SOLEP PREMIER HI GRO

Manufacturer
Kobizstar Co., Ltd. | Ester Co., Ltd.
Effective date
2020-11-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:48

Label at a glance#

ProductSOLEP PREMIER HI GRO
Active ingredientPanthenol, PYRITHIONE ZINC, Salicylic Acid
Label structure10 sections

Dosage and administration

Use 1 time per day as following. 1) Wet hair and scalp with lukewarm water 2) Apply adequate amount and work lather on hair and scalp. 3) Rinse thoroughly after 2-3 minutes.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Panthenol 0.50%
Zinc Pyrithione 0.30%
Salicylic Acid 0.20%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Potassium Cocoyl Glycinate, Lauryl Glucoside, Lauramidopropyl Betaine, Cocamide MIPA, Tetrasodium EDTA, 1,2-Hexanediol, Illicium Verum (Anise) Fruit Extract, Scutellaria Baicalensis Root Extract, Butylene Glycol, Pantolactone, Polyquaternium-10, Menthol, Citric Acid, Coptis Japonica Root Extract, Rhizophora Mangle Callus Culture Extract, Eucalyptus Globulus Leaf Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Lavandula Angustifolia (Lavender) Oil, 1,2-Hexanediol, Ethylhexylglycerin, Aloe Barbadensis Leaf Extract, Opuntia Coccinellifera Fruit Extract, Schisandra Chinensis Fruit Extract, Aronia Arbutifolia Extract, Cordyceps Sinensis Extract, Sparassis Crispa Extract, Dioscorea Japonica Root Extract, Albumen Extract, Hydrolyzed Ginseng Saponins, Saponaria Officinalis Leaf Extract, Hydrolyzed Silk, Hydrolyzed Elastin, Hydrolyzed Keratin, Limonene, Linalool

PURPOSE

OTC - PURPOSE SECTION

Anti-hairloss

WARNINGS

WARNINGS SECTION

1. Consult with a specialist if there are any abnormal symptoms or side effects such as red spots, swelling or itching when using or after use in direct sunlight. 2. Avoid using on wounded areas. 3. Precautions for storage and handling A) Keep out of reach of children. B) Store away from direct sunlight. 4. In case of eye contact, wash it off immediately. 5. It may cause hair loss or discoloration if not washed off with water after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Use(s)

INDICATIONS & USAGE SECTION

■ Helps relieve hair loss.

Directions

DOSAGE & ADMINISTRATION SECTION

Use 1 time per day as following.
1) Wet hair and scalp with lukewarm water
2) Apply adequate amount and work lather on hair and scalp.
3) Rinse thoroughly after 2-3 minutes.

Other Information

OTHER SAFETY INFORMATION

■ If any defect in this product, you are compensated in accordance with “Consumer Dispute Resolution Criteria” notified by Fair Trade Commission.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81077-010-022025-01-30C16284748780-12cef2736-b6c9-d83d-e063-dadaa90ab31f5ae01fd8-8a20-4c24-8d8d-4de491a72f80

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81077-010-01SOLEP PREMIER HI GRO300 mL in 1 BOTTLESHAMPOO3001
81077-010-02SOLEP PREMIER HI GRO1 in 1 CARTONSHAMPOO11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81077-010SOLEP PREMIER HI GRO (PANTHENOL, ZINC PYRITHIONE, SALICYLIC ACID) SHAMPOO [KOBIZSTAR CO., LTD.]1Legacy NDC, 2 package rows20201118_5ae01fd8-8a20-4c24-8d8d-4de491a72f80.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
81077-01081077-010-01, 81077-010-02

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
5992e67f-12df-42a8-b427-35cc6828e3735ae01fd8-8a20-4c24-8d8d-4de491a72f802020-11-17WarningsExact identifier
spl id: 5992e67f-12df-42a8-b427-35cc6828e373
spl set id: 5ae01fd8-8a20-4c24-8d8d-4de491a72f80

Reported adverse events (FAERS/openFDA)#

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