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Plant Stemcell VEGF bFGF Tonic

Dosage form: liquid
Ingredients: ALLANTOIN 0.1g in 100mL
Labeler: Humajor Co., Ltd.
NDC Code: 69244-2001

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


water, Alcohol ,  1,2-Hexanediol , Propanediol , Pisum Sativum (Pea) Peptide , Nelumbo Nucifera Callus Culture Extract ,  Lecithin ,  Sodium Hyaluronate ,  rh-Oligopeptide-1  , Moringa Pterygosperma Seed Extract  , Allantoin , Hippophae Rhamnoides Extract, Tocopheryl Acetate  ,Panthenol, Pyrrolidinyl Diaminopyrimidine Oxide  , Biotin, Sodium Chloride  , PEG-60 Hydrogenated Castor Oil   , Fragrance


hair growth and loss prevention


keep out or reach of the children


Apply the solution to the scalp daily and gently massage the scalp to promote absorption


1) Discontinue using this product if symptoms listed below occurs. If conitued the condition may worsen. Speak to your dermatologist prior to resuming use. 
A) Rash, Red Spotting, Itchiness or edema occurs after use
B) If applied area has symptoms as below when exposed to direct sunlight
2) Do not use on areas with wounds, skin irritations, eczma and on cracked skin.
3) Storage Instructions and Usage precautions
A) Securely close the lid after use
B) Keep out of reach of children
C) Do not store in places of high or low temperature or expossed to direct sunlight.


for external use only


PLANT STEMCELL VEGF BFGF TONIC 
allantoin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69244-2001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (ALLANTOIN) ALLANTOIN0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYALURONATE SODIUM 
SODIUM CHLORIDE 
PANTHENOL 
Packaging
#Item CodePackage Description
1NDC:69244-2001-1120 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34710/01/2014
Labeler - Humajor Co., Ltd. (689061827)
Registrant - Humajor Co., Ltd. (689061827)
Establishment
NameAddressID/FEIOperations
Humajor Co., Ltd.689061827manufacture(69244-2001)

Revised: 08/2016
 
Humajor 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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