Label: MONPURIEL DAILY ALL IN ONE AMPLE- l-menthol, dexpanthenol, salicylic acid liquid
- NDC Code(s): 83472-311-01
- Packager: Y2K 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 January 4, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purposes
- Uses
- Warnings
- Warnings
- Warnings
- Warnings
- Warnings
- Directions
-
Inactive Ingredients
Dipropylene Glycol, Glycerin, Butylene Glycol, Water, 1,2-Hexanediol, Propanediol, Panthenol, Dipotassium Glycyrrhizate, Tromethamine, Xanthan Gum, Carbomer, PEG-60 Hydrogenated Castor Oil, Allantoin, Adenosine,
Glyceryl Acrylate/Acrylic Acid Copolymer, Lavandula Angustifolia (Lavender) Oil (Allergens : Geraniol, Limonene, Linalool),
Sodium Hyaluronate, Beta-Glucan, Phosphate buffered saline, Cynanchum Atratum Extract, Lactobacillus Extracellular Vesicles,
sh-Oligopeptide-1, Ethylhexylglycerin, Lycium Chinense Fruit Extract
- Label
-
INGREDIENTS AND APPEARANCE
MONPURIEL DAILY ALL IN ONE AMPLE
l-menthol, dexpanthenol, salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83472-311 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL 0.33 g in 100 mL DEXPANTHENOL (UNII: 1O6C93RI7Z) (DEXPANTHENOL - UNII:1O6C93RI7Z) DEXPANTHENOL 0.22 g in 100 mL SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.25 g in 100 mL Inactive Ingredients Ingredient Name Strength LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5) CENTELLA ASIATICA LEAF (UNII: 6810070TYD) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) PANTHENOL (UNII: WV9CM0O67Z) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) TROMETHAMINE (UNII: 023C2WHX2V) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) ALLANTOIN (UNII: 344S277G0Z) ADENOSINE (UNII: K72T3FS567) LAVENDER OIL (UNII: ZBP1YXW0H8) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER (300000 CP AT 2%) (UNII: MEA9KH24QG) SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP) LYCIUM CHINENSE FRUIT (UNII: TG711Q7A1Q) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) PROPANEDIOL (UNII: 5965N8W85T) VINCETOXICUM ATRATUM WHOLE (UNII: U3176B0S5J) NEPIDERMIN (UNII: TZK30RF92W) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) DIPROPYLENE GLYCOL (UNII: E107L85C40) XANTHAN GUM (UNII: TTV12P4NEE) PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83472-311-01 30 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2023 Labeler - Y2K Co., Ltd. (695705051) Registrant - Y2K Co., Ltd. (695705051) Establishment Name Address ID/FEI Business Operations Y2K Co., Ltd. 695705051 manufacture(83472-311)