Label: NON-SHEET SERUMST- glycerin, allantoin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72943-0003-1 - Packager: DAONMEDICOS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 Label Information
Updated March 24, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
■ 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
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
NON-SHEET SERUMST
glycerin, allantoin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72943-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALLANTOIN (UNII: 344S277G0Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72943-0003-1 130 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/24/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 03/24/2019 Labeler - DAONMEDICOS CO. (694819928) Registrant - DAONMEDICOS CO. (694819928) Establishment Name Address ID/FEI Business Operations DAONMEDICOS CO. 694819928 manufacture(72943-0003) , label(72943-0003) , pack(72943-0003)
