NON-SHEET SERUMST- glycerin, allantoin liquid 
DAONMEDICOS CO.

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

Sea Water
Water
Butylene Glycol
Glycerin
Niacinamide
Saccharomyces/Artemisia Princeps Leaf Ferment Filtrate
Elaeagnus Glabra Extract
Pentylene Glycol
Hexacarboxymethyl Dipeptide-12
Dipotassium Glycyrrhizate
Gellan Gum
rh-Oligopeptide-1
sh-Decapeptide-7
sh-Octapeptide-4
sh-Oligopeptide-9
sh-Pentapeptide-19
Digalloyl Tetrapeptide-19
Tripeptide-48
Nicotinoyl Tripeptide-1
Palmitoyl Pentapeptide-4
Ovalicin
Propanediol
Nonapeptide-29 Hexapeptide-8
Nonapeptide-29 Pentapeptide-4
Isopentyldiol
Polyglyceryl-4 Oleate
Sucrose Palmitate
Ceramide NP
Propanediol
Butylene Glycol
Portulaca Oleracea Extract
Centella Asiatica Extract
Adenosine
Disodium EDTA
Allantoin
Panthenol
Betaine
Sodium Chloride
Water
Human Adipocyte Conditioned Media Extract
Phytosphingosine
Ceramide NP
Phospholipids
Caprylyl Glycol
Tropolone
Phytosterols
Squalane
1,2-Hexanediol

whitening

anti-wrinkle

keep out of reach of the children

spread evenly over the skin

■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

for external use only

label

NON-SHEET SERUMST 
glycerin, allantoin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72943-0003
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
WATER (UNII: 059QF0KO0R)  
ALLANTOIN (UNII: 344S277G0Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72943-0003-1130 mL in 1 BOTTLE; Type 0: Not a Combination Product03/24/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34703/24/2019
Labeler - DAONMEDICOS CO. (694819928)
Registrant - DAONMEDICOS CO. (694819928)
Establishment
NameAddressID/FEIBusiness Operations
DAONMEDICOS CO.694819928manufacture(72943-0003) , label(72943-0003) , pack(72943-0003)

Revised: 3/2019
Document Id: 84d1b350-df6e-8c0c-e053-2a91aa0ad73f
Set id: 84d1b30e-f962-5138-e053-2991aa0a9406
Version: 1
Effective Time: 20190324
 
DAONMEDICOS CO.