REEN HAIRLOSS CLINIC JAHAJIN SHAMPOO FOR SENSITIVE SCALP - pyrithione zinc, panthenol, niacinamide liquid 
LG Household and Healthcare, Inc.

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.

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Drug Fact

PYRITHIONE ZINC 1%

PANTHENOL 0.2%

NIACINAMIDE 0.1%

For external use only.

 Keep out the reach of children.

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.

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Clinic for Sensitive Scalp.

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Reen Shampoo

REEN HAIRLOSS CLINIC JAHAJIN SHAMPOO FOR SENSITIVE SCALP 
pyrithione zinc, panthenol, niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-516
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC1 mL  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.1 mL  in 100 mL
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL0.2 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53208-516-01400 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/02/2011
Labeler - LG Household and Healthcare, Inc. (688276187)
Registrant - LG Household and Healthcare, Inc. (688276187)
Establishment
NameAddressID/FEIBusiness Operations
LG Household and Healthcare, Inc.688276187manufacture

Revised: 4/2011
Document Id: 10794c21-542e-479a-8266-64cdae9dc30d
Set id: d8e3052c-9b2c-44c3-a09e-ed9b8d79b512
Version: 2
Effective Time: 20110406
 
LG Household and Healthcare, Inc.