Label: REEN HAIRLOSS CLINIC JAHAJIN SHAMPOO FOR SENSITIVE SCALP- pyrithione zinc, panthenol, niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 53208-516-01 - Packager: LG Household and Healthcare, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 6, 2011
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- ACTIVE INGREDIENT
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
WATER, SODIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, COCO MONOETHANOLAMIDE, GLYCOL DISTEARATE, DIMETHICONE, POLYQUATERNIUM-10 (400 CPS AT 2%), CHLORIDE ION, LAURETH-4, LAURETH-23, SOPHORA FLAVESCENS ROOT, ASARUM SIEBOLDII ROOT, COPTIS JAPONICA ROOT, REISHI, SODIUM CITRATE, CITRIC ACID MONOHYDRATE, EDETATE SODIUM, SODIUM CHLORIDE, HEXYLENE GLYCOL, SODIUM BENZOATE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, METHYLPARABEN, CARAMEL, MENTHOL.
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
REEN HAIRLOSS CLINIC JAHAJIN SHAMPOO FOR SENSITIVE SCALP
pyrithione zinc, panthenol, niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-516 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 mL in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 0.1 mL in 100 mL PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.2 mL in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) COCO MONOETHANOLAMIDE (UNII: C80684146D) GLYCOL DISTEARATE (UNII: 13W7MDN21W) DIMETHICONE (UNII: 92RU3N3Y1O) POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS) CHLORIDE ION (UNII: Q32ZN48698) LAURETH-4 (UNII: 6HQ855798J) LAURETH-23 (UNII: N72LMW566G) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) ASARUM SIEBOLDII ROOT (UNII: 8IPR99RALA) COPTIS JAPONICA ROOT (UNII: JH0SWT16D1) REISHI (UNII: TKD8LH0X2Z) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM CHLORIDE (UNII: 451W47IQ8X) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM BENZOATE (UNII: OJ245FE5EU) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM BENZOATE (UNII: OJ245FE5EU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) METHYLPARABEN (UNII: A2I8C7HI9T) CARAMEL (UNII: T9D99G2B1R) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53208-516-01 400 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/02/2011 Labeler - LG Household and Healthcare, Inc. (688276187) Registrant - LG Household and Healthcare, Inc. (688276187) Establishment Name Address ID/FEI Business Operations LG Household and Healthcare, Inc. 688276187 manufacture
