Label: SKINBUTAK GO YOUNG MAGIC TONER- glycerin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81851-203-01 - Packager: NatureBlue Co.,Ltd
- 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 April 28, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask doctor if
- Keep out of reach of children
- Directions
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Inactive Ingredients
Hippophae Rhamnoides Fruit Extract, Niacinamide, Glycerin, Polyglyceryl-6 Caprylate, Polyglyceryl-4 Caprate, 1, 2-Hexanediol, Arginine, Carbomer, Dipropylene Glycol, Sodium Hyaluronate, Glycyrrhiza Glabra (Licorice) Root Extract, Zingiber Officinale (Ginger) Root Extract, Schisandra Chinensis Fruit Extract, Coptis Japonica Root Extract, Camellia Sinensis Leaf Extract, Propolis Wax, Butylene Glycol, Asiaticoside, Caprylyl Glycol, Xanthan Gum, Allantoin, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Oil, Citrus Paradisi (Grapefruit) Peel Oil, Citrus Tangerina (Tangerine) Peel Oil, Eucalyptus Globulus Leaf Oil, Lavandula Angustifolia (Lavender) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Sodium Citrate, Adenosine, Disodium EDTA, Citric Acid, Hippophae Rhamnoides Fruit Oil, Diospyros Kaki Leaf Extract, Morus Alba Bark Extract, Sophora Angustifolia Root Extract, Pueraria Lobata Root Extract, Pinus Palustris Leaf Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Thuja Orientalis Extract, Ulmus Davidiana Root Extract, Taraxacum Officinale (Dandelion) Extract
- Other Information
- Package Label
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INGREDIENTS AND APPEARANCE
SKINBUTAK GO YOUNG MAGIC TONER
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81851-203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2 mg in 100 mL ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 0.8 mg in 100 mL Inactive Ingredients Ingredient Name Strength HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) CAPRYLYL GLYCOL (UNII: 00YIU5438U) NIACINAMIDE (UNII: 25X51I8RD4) DIPROPYLENE GLYCOL (UNII: E107L85C40) SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ARGININE (UNII: 94ZLA3W45F) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) COPTIS JAPONICA ROOT (UNII: JH0SWT16D1) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ASIATICOSIDE (UNII: PKO39VY215) ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B) GRAPEFRUIT OIL (UNII: YR377U58W9) MANDARIN OIL (UNII: NJO720F72R) ROSEMARY OIL (UNII: 8LGU7VM393) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) MORUS ALBA BARK (UNII: 7O71A48NDP) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) PINUS PALUSTRIS LEAF (UNII: OT6R5143A1) OENOTHERA BIENNIS FLOWER (UNII: Y1YXJ1M6Z5) POLYGLYCERYL-6 CAPRYLATE (UNII: DGV8R54VG7) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GINGER (UNII: C5529G5JPQ) PROPOLIS WAX (UNII: 6Y8XYV2NOF) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EUCALYPTUS OIL (UNII: 2R04ONI662) LAVENDER OIL (UNII: ZBP1YXW0H8) ADENOSINE (UNII: K72T3FS567) HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J) DIOSPYROS KAKI LEAF (UNII: Q71GF9OBNO) PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C) ULMUS DAVIDIANA ROOT (UNII: URQ79U8261) TARAXACUM OFFICINALE (UNII: 39981FM375) XANTHAN GUM (UNII: TTV12P4NEE) BERGAMOT OIL (UNII: 39W1PKE3JI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81851-203-01 120 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/28/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 04/28/2021 Labeler - NatureBlue Co.,Ltd (689062549) Registrant - NatureBlue Co.,Ltd (689062549) Establishment Name Address ID/FEI Business Operations NatureBlue Co.,Ltd 689062549 manufacture(81851-203)
