Label: PEONY ACMELLA ANTIOXIDANT SERUM- allantoin, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73307-0001-1 - Packager: TOM Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 19, 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
Water
Propanediol
Glycereth-26
1,2-Hexanediol
Acmella Oleracea Extract
Paeonia Albiflora Flower Extract
Butylene glycol
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Glucose
Carrageenan
Camellia Sinensis Leaf Extract
Aspalathus Linearis Extract
Euterpe Oleracea Fruit Extract
Aronia Melanocarpa Fruit Extract
Tromethamine
Disodium EDTA - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
Precautions
Please stop using this product ifthe following side effects occur.If not, its symptom is worsened.
Then please consultdermatologist about it.
1) If it is occurred red spots,itching, stimulation, and others.
2) If it is occurred side effectsas above on the applied partby direct sunlight.
Please avoid to be applied it onthe wounded part and the part ofeczema and dermatitis.
Warnings in storage andmaintenance.
1) Close a lid after using it.
2) Keep it out of children’s reach.
3) Don’t keep it in hightemperature or in direct sunlight.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PEONY ACMELLA ANTIOXIDANT SERUM
allantoin, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73307-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.1 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73307-0001-1 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/17/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/17/2019 Labeler - TOM Co., Ltd. (690387164) Registrant - TOM Co., Ltd. (690387164) Establishment Name Address ID/FEI Business Operations TOM Co., Ltd. 690387164 label(73307-0001) , pack(73307-0001) Establishment Name Address ID/FEI Business Operations AINCOS LTD 694204651 manufacture(73307-0001)
