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Queen Perfume Hair Conditioner

Medically reviewed on January 30, 2018.

Dosage form: liquid
Ingredients: ALLANTOIN 0.02mg in 1mL
Labeler: Tamnamo Co., Ltd
NDC Code: 60344-6001

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 Facts

allantoin


Jeju Water, Cetearyl alcohol, Cetrimoniumchloride, Dimethicone and Laureth-23 and Laureth-3, SOYAMIDE DEA QUATERNIUM-52 POLYQUATERNIUM-11 MAGNESIUM NITRATE MAGNESIUM CHLORIDE, Glyceryl Stearate SE, PEG-10 Sorbitan Laurate , Acrus Calamus Root Extrct, Lawsonia Inermis Extract, Kumsong Extract, Sophora Flavescens Root Extract, Angelica Gigas Root Extract, Soluble Seaweed Extract, Glycyrrhiza  Glabra (Licorice)Root Extract, Witch Hazel Extract, Espinosilla Extract, Red Ginseng Extract, Duchesnea Indica Fruit Extract, Sodium Cocoyl Hydrolyzed Wheat Protein, Polyquaternium 10, Camellia Japonica Seed Oil, D-Panthenol, Allantoin, Hydrolyzed Silk, Sodium Hyaluronate, Tocopheryl Acetate, Rosmarinus Officinalis, Disodium EDTA, Perfume, Zanthoxylum Pieperitum Fruit Extract, Pulsatilla Koreana Extract, Usnea Barbata Root Extract



supplying moisture and nutrient to scalp and hair



keep out of reach of the children

after shampooing, work evenly into wet hair with fingertips, paying special attention to ends or damaged areas
rinse thoroughly



stop use if irritation occurs
avoid contact with eyes


for external use only

QUEEN PERFUME HAIR CONDITIONER 
allantoin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60344-6001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN0.02 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL 
GLYCERYL MONOSTEARATE 
SOPHORA FLAVESCENS ROOT 
ANGELICA GIGAS ROOT 
GLYCYRRHIZA GLABRA 
HYALURONATE SODIUM 
Packaging
#Item CodePackage Description
1NDC:60344-6001-1355 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34701/30/2014
Labeler - Tamnamo Co., Ltd (688732377)
Registrant - Tamnamo Co., Ltd (688732377)
Establishment
NameAddressID/FEIOperations
Tamnamo Co., Ltd688732377manufacture(60344-6001)

 
Tamnamo Co., Ltd

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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