Label: YVTYVT MICRODERMABRASION FACIAL SCRUB ointment

  • NDC Code(s): 85212-0018-1
  • Packager: Beijing JUNGE Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 28, 2025

If you are a consumer or patient please visit this version.

  • DOSAGE & ADMINISTRATION

    NET WT. 30 G /1 OZ

  • INDICATIONS & USAGE


    1. Apply to clean skin.

    2. Gently massage a liberal amount of exfoliating scrub onto damp skin in circular motions.

    3. Rinse thoroughly with water to reveal fresh and radiant skin.

  • PRECAUTIONS

    1.For External Use Only.

    2.Avoid Direct Contact with Eyes.

    3.If the product gets into your eyes, rinse immediately with plenty of water.

    4.Discontinue Use if Irritation Occurs: If redness, itching, or irritation develops, stop use and consult a dermatologist.

    5.Do Not Apply on Broken or Irritated Skin.

  • INACTIVE INGREDIENT

    AQUA
    BUTYLENE GLYCOL
    PROPYLENE GLYCOL
    CETEARYL ALCOHOL
    ETHYLHEXYL PALMITATE
    LACTIC ACID
    SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL
    STEARIC ACID
    PEG-100 STEARATE
    GLYCERYL STEARATE
    PEG-20 METHYL GLUCOSE SESQUISTEARATE
    BEHENYL ALCOHOL
    TOCOPHEROL
    CAMELLIA SINENSIS LEAF EXTRACT
    CHRYSANTHELLUM INDICUM EXTRACT
    ALOE BARBADENSIS LEAF EXTRACT
    HYDROXYPROPYL METHYLCELLULOSE
    CLADOSIPHON OKAMURANUS EXTRACT
    CARBOMER
    XANTHAN GUM
    1,2-HEXANEDIOL
    ALLANTOIN
    GLYCERYL CAPRYLATE

  • PURPOSE

    Exfoliate, deeply cleanse pores and stimulate the skin's metabolism.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • WARNINGS

    For external use only. Keep out of reach of children.Avoid contact with eyes.

  • PRINCIPAL DISPLAY PANEL

    MICRODERMABRASION FACIAL SCRUB

  • INGREDIENTS AND APPEARANCE
    YVTYVT MICRODERMABRASION FACIAL SCRUB 
    yvtyvt microdermabrasion facial scrub ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85212-0018
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) (MICROCRYSTALLINE CELLULOSE - UNII:OP1R32D61U) MICROCRYSTALLINE CELLULOSE3 g  in 100 g
    BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) (BUTYROSPERMUM PARKII (SHEA) BUTTER - UNII:K49155WL9Y) BUTYROSPERMUM PARKII (SHEA) BUTTER3 g  in 100 g
    BEESWAX (UNII: 2ZA36H0S2V) (BEESWAX - UNII:2ZA36H0S2V) BEESWAX1 g  in 100 g
    BETAINE (UNII: 3SCV180C9W) (BETAINE - UNII:3SCV180C9W) BETAINE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 5 g  in 100 g
    PEG-100 STEARATE (UNII: YD01N1999R) 1 g  in 100 g
    TOCOPHEROL (UNII: R0ZB2556P8) 0.5 g  in 100 g
    XANTHAN GUM (UNII: TTV12P4NEE) 0.1 g  in 100 g
    SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M) 2 g  in 100 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 1 g  in 100 g
    LACTIC ACID (UNII: 33X04XA5AT) 2 g  in 100 g
    CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0) 0.5 g  in 100 g
    GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) 0.1 g  in 100 g
    ETHYLHEXYL PALMITATE (UNII: 2865993309) 2 g  in 100 g
    ALLANTOIN (UNII: 344S277G0Z) 0.1 g  in 100 g
    BEHENYL ALCOHOL (UNII: 9G1OE216XY) 0.5 g  in 100 g
    CARBOMER (UNII: 0A5MM307FC) 0.1 g  in 100 g
    1,2-HEXANEDIOL (UNII: TR046Y3K1G) 0.1 g  in 100 g
    CHRYSANTHELLUM INDICUM WHOLE (UNII: YPX537PA31) 0.2 g  in 100 g
    GLYCERYL STEARATE (UNII: 230OU9XXE4) 1 g  in 100 g
    ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) 0.2 g  in 100 g
    HYDROXYPROPYL METHYLCELLULOSE (UNII: 3NXW29V3WO) 0.2 g  in 100 g
    CLADOSIPHON OKAMURANUS WHOLE (UNII: 2IJE0CH09J) 0.1 g  in 100 g
    PEG-20 METHYL GLUCOSE SESQUISTEARATE (UNII: 0345752X7U) 1 g  in 100 g
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 5 g  in 100 g
    AQUA (UNII: 059QF0KO0R) 65.3 g  in 100 g
    CETEARYL ALCOHOL (UNII: 2DMT128M1S) 3 g  in 100 g
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85212-0018-130 g in 1 BOTTLE; Type 0: Not a Combination Product01/10/2025
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/10/2025
    Labeler - Beijing JUNGE Technology Co., Ltd. (848718652)
    Registrant - Beijing JUNGE Technology Co., Ltd. (848718652)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Ayan Biotech Co., Ltd.544377996manufacture(85212-0018)