HASOL ANTI HAIR LOSS DAY TONIC- salicylic acid,niacinamide liquid

Hasol Anti hair loss day tonic by

Drug Labeling and Warnings

Hasol Anti hair loss day tonic by is a Otc medication manufactured, distributed, or labeled by Ecomine Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Ha'sol Anti hair loss day tonic

Salicylic acid (0.5%) --------------------------------------------------------------------- antiseborrheicNiacinamide (0.3%) ---------------------------------------------------------------------------- hair tonic

Uses To strengthen hair root, give growth stimulation and thicken hair

Keep out of reach of childrenDo not swallow. In case of accidental ingestion, seek professional assistance

After shampoo, massage the scalp in order to be absorbed fully focusing on the part of hair loss. Do not rinse off after application since it is a hair loss preventing and hair tonic product.

For external use onlyDo not use when Your scalp is red, inflamed, irritated or painful When using this product Do not apply on other parts of the body Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not apply directly to wound or open cut. Stop use and ask doctor if rash or irritation on scalp develops and lasts. Keep out of reach of children Do not swallow. In case of accidental ingestion, seek professional assistance. Store at room temperature

After shampoo, massage the scalp in order to be absorbed fully focusing on the part of hair loss. Do not rinse off after application since it is a hair loss preventing and hair tonic product.

Water, Alcohol, Equisetum Arvense Extract,Salvia Officinalis (Sage) Extract, Zingiber Officinale(Ginger) Root Extract, Camellia Sinensis Leaf Extract, PEG-60 Hydrogenated Castor Oil, Panax Ginseng Root Extract, Propylene Glycol, Salicylic Acid, Niacinamide, Fragrance

INGREDIENTS AND APPEARANCE

HASOL ANTI HAIR LOSS DAY TONIC 
salicylic acid,niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51270-117
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	Salicylic Acid	0.375 g  in 75 g
Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	Niacinamide	0.225 g  in 75 g

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
Alcohol (UNII: 3K9958V90M)
EQUISETUM ARVENSE WHOLE (UNII: 73DM367W4P)
SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E)
ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)
Propylene Glycol (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51270-117-02	15 in 1 BOX
1	NDC: 51270-117-01	5 g in 1 AMPULE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2014

Labeler - Ecomine Co., Ltd. (557795691)

Registrant - Ecomine Co., Ltd. (557795691)

Establishment
Name	Address	ID/FEI	Business Operations
Ecomine Co., Ltd.		557795691	manufacture(51270-117)