Label: HASOL ANTI HAIR LOSS DAY TONIC- salicylic acid,niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 51270-117-01, 51270-117-02 - Packager: Ecomine Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 24, 2013
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- Official Label (Printer Friendly)
- 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
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INGREDIENTS AND APPEARANCE
HASOL ANTI HAIR LOSS DAY TONIC
salicylic acid,niacinamide liquidProduct 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)