Label: MARINE PURIFYING- panthenol, allantoin patch
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Contains inactivated NDC Code(s)
NDC Code(s): 71727-102-01, 71727-102-02, 71727-102-03 - Packager: iMode Korea, Inc.
- 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 February 7, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- Directions
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Inactive ingredients
Water, Glycerin, Dipropylene Glycol, Castanea Crenata (Chestnut) Shell Extract, Moringa Pterygosperma Seed Extract, Malva Sylvestris (Mallow) Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Alchemilla Vulgaris Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Achillea Millefolium Extract, Alcohol, Sodium Hydroxide, Eucalyptus Globulus Leaf Extract, Scutellaria Baicalensis Root Extract, Ethylhexylglycerin, Glyceryl Caprylate, Fucus Vesiculosus Extract, Prunella Vulgaris Extract, Sodium Hyaluronate, Butylene Glycol, PEG-32, Trehalose, Sodium Lactate, PEG-2M, Silica, Sodium Citrate, Xanthan Gum, PEG-60 Hydrogenated Castor Oil, Glyceryl Acrylate/Acrylic Acid Copolymer, Propylene Glycol, Caprylyl Glycol, Caffeine, Hydroxyethylcellulose, Cyclodextrin, Dextrin, Cellulose Gum, Disodium EDTA, Hydroxyacetophenone, Hexylene Glycol, Caprylhydroxamic Acid, Propanediol, Ethyl Hexanediol, 1,2-Hexanediol, Chlorphenesin
- MARINE PURIFYING
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INGREDIENTS AND APPEARANCE
MARINE PURIFYING
panthenol, allantoin patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71727-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.162 mg in 27 mL ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.081 mg in 27 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CASTANEA CRENATA SHELL (UNII: MTF3V701OO) MALVA SYLVESTRIS FLOWERING TOP (UNII: X1U1U0N90J) MENTHA PIPERITA LEAF (UNII: A389O33LX6) PRIMULA VERIS (UNII: W6LFQ57E4M) ALCHEMILLA XANTHOCHLORA FLOWERING TOP (UNII: 9M289NKI69) DIPROPYLENE GLYCOL (UNII: E107L85C40) MORINGA OLEIFERA SEED (UNII: TIX5482832) MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) ALCOHOL (UNII: 3K9958V90M) SODIUM HYDROXIDE (UNII: 55X04QC32I) EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) FUCUS VESICULOSUS (UNII: 535G2ABX9M) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71727-102-03 5 in 1 BOX 01/03/2018 1 NDC:71727-102-02 1 in 1 POUCH 1 NDC:71727-102-01 27 mL in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/03/2018 Labeler - iMode Korea, Inc. (694627846) Registrant - iMode Korea, Inc. (694627846) Establishment Name Address ID/FEI Business Operations JINCOSTECH Co., Ltd. 688484870 manufacture(71727-102) Establishment Name Address ID/FEI Business Operations iMode Korea, Inc. 694627846 relabel(71727-102)
