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FOLLIGEN by Humajor Co., Ltd.

Dosage form: shampoo
Ingredients: PYRITHIONE ZINC 2.1g in 100mL
Labeler: Humajor Co., Ltd.
NDC Code: 69244-4001

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


Water, Sodium Laureth Sulfate , Ammonium Lauryl Sulfate,  Cocamidopropyl Betaine, Glycerin,Polyquaternium-7,  Dimethicone, Zinc Pyrithione,  Cocamide DEA,  Panthenol,   Guar Hydroxypropyltrimonium Chloride, Niacinamide,  Menthol,  Cetrimonium Chloride,  Zinc Chloride,  Biotin, Trideceth-10, Sodium Polynaphthalenesulfonate, Butylene Glycol, Sophora Angustifolia Root Extract , Glycyrrhiza Glabra (Licorice) Root Extract, Coix Lacryma-Jobi Ma-yuen Seed Extract, Artemisia Princeps Leaf Extract, Carbomer,Sodium Chloride,  Disodium EDTA,  Citric Acid,  Sodium Benzoate, Phenoxyethanol,Fragrance

hair growth and loss prevention

keep out or reach of the children

Moisten hair and scalp with warm water enough. And with 3~5ml of it, massage the scalp evenly. With hair covered with foam, wait for over 3 miniutes. And wash it away

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult ypur phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

for external use only

pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69244-4001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:69244-4001-1500 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H10/01/2014
Labeler - Humajor Co., Ltd. (689061827)
Registrant - Humajor Co., Ltd. (689061827)
Humajor Co., Ltd.689061827manufacture(69244-4001)

Revised: 08/2016
Humajor Co., Ltd.

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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.