PLANT STEMCELL VEGF BFGF TONIC- allantoin liquid 
Humajor Co., Ltd.

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.

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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


package label
PLANT STEMCELL VEGF BFGF TONIC 
allantoin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69244-2001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PANTHENOL (UNII: WV9CM0O67Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69244-2001-1120 mL in 1 BOTTLE; Type 0: Not a Combination Product08/08/201605/08/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34710/01/201405/08/2018
Labeler - Humajor Co., Ltd. (689061827)
Registrant - Humajor Co., Ltd. (689061827)
Establishment
NameAddressID/FEIBusiness Operations
Humajor Co., Ltd.689061827manufacture(69244-2001)

Revised: 5/2018
 
Humajor Co., Ltd.