Label: HASOL INTENSIVE- salicylic acid shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 51270-119-01, 51270-119-02 - Packager: Ecomine Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 18, 2014
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- Official Label (Printer Friendly)
- HA'SOL Intensive Shampoo
- Salicylic acid (0.2%)
- Anti-dandruff
- Keep out of reach of childrenDo not swallow. In case of accidental ingestion, seek professional assistance.
- To recover the scalp condition for healthier hair
- For external use only Do not use when Your scalp is red, inflamed, irritated or painful. When using this productDo not apply on other parts of the bodyAvoid 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. Store at room temperature
- Directions After shampoo, massage the scalp for 2-3 minutes. Rinse off after application.
- Inactive Ingredients Water, Ammonium Lauryl Sulfate, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Glycerin, Propylene Glycol, Phyllanthus Emblica Fruit Extract, Camellia Sinensis Leaf Extract, Tribulus Terrestris Fruit Extract, Laureth-2, Laureth-23, Dimethicone, Dimethiconol, Panax Ginseng Root Extract, Glycol Stearate, Polyquaternium-10, Lauramide DEA, Betaine, Trihydroxystearin, Fragrance, Cetyl Alcohol, Niacinamide, Menthol, Tocopheryl Acetate, Zingiber Officinale (Ginger) Root Extract, Equisetum Arvense Extract, Urtica Dioica (Nettle) Extract, Salvia Officinalis (Sage) Extract, Serenoa Serrulata Fruit Extract, Methychloroisothiazolinone/Methyisothiazolinone, Disodium EDTA, Laminaria Japonica Extract
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INGREDIENTS AND APPEARANCE
HASOL INTENSIVE
salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51270-119 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.1 in 300 mL Inactive Ingredients Ingredient Name Strength NIACINAMIDE (UNII: 25X51I8RD4) WATER (UNII: 059QF0KO0R) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576) GREEN TEA LEAF (UNII: W2ZU1RY8B0) TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ) LAURETH-2 (UNII: D4D38LT1L5) LAURETH-23 (UNII: N72LMW566G) DIMETHICONE (UNII: 92RU3N3Y1O) DIMETHICONOL (100000 CST) (UNII: OSA9UP217S) ASIAN GINSENG (UNII: CUQ3A77YXI) GLYCOL STEARATE (UNII: 0324G66D0E) POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK) LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38) BETAINE (UNII: 3SCV180C9W) TRIHYDROXYSTEARIN (UNII: 06YD7896S3) CETYL ALCOHOL (UNII: 936JST6JCN) MENTHOL (UNII: L7T10EIP3A) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GINGER (UNII: C5529G5JPQ) EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) URTICA DIOICA LEAF (UNII: X6M0DRN46Q) SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E) SAW PALMETTO (UNII: J7WWH9M8QS) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) EDETATE DISODIUM (UNII: 7FLD91C86K) LAMINARIA JAPONICA (UNII: WE98HW412B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51270-119-02 1 in 1 CARTON 1 NDC:51270-119-01 300 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 08/20/2014 Labeler - Ecomine Co., Ltd. (557795691) Registrant - Ecomine Co., Ltd. (557795691) Establishment Name Address ID/FEI Business Operations Ecomine Co., Ltd. 557795691 manufacture(51270-119)