PLANT STEMCELL VEGF BFGF AMPLE- glycerin 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

glycerin


Bambusa Vulgaris Water, Butylene Glycol, Alcohol, Glycerin, 1,2-Hexanediol, Nelumbo Nucifera Callus Culture Extract, Propanediol, Pisum Sativum (Pea) Peptide, Moringa Pterygosperma Seed Extract, sh-Polypeptide-9, Polysorbate 20, Lecithin, sh-Polypeptide-1, Allantoin, Panthenol, Tocopheryl Acetate, Pyrrolidinyl diaminopyrimidine oxide, Sodium Polyacrylate, Hydroxyethylcellulose, PEG-60 Hydrogenated Castor Oil, Phenoxyethanol, Fragrance


hair growth and loss prevention


keep out or reach of the children


Gently massage into the scalp using the fingertips to allow the scalp to absorb the solution. Use once or twice a week


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 AMPLE 
glycerin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69244-3001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PANTHENOL (UNII: WV9CM0O67Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69244-3001-210 in 1 BOX08/08/201605/08/2018
1NDC:69244-3001-15 mL in 1 BOTTLE; Type 0: Not a Combination Product
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(69244-3001)

Revised: 5/2018
 
Humajor Co., Ltd.