Label: BLOOMELLEE 14%GEL AZELAIC ACID CREAM- 14%azelaic acid cream

  • NDC Code(s): 87386-002-01
  • Packager: Shenzhen Lanxi Trading Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 2, 2026

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

  • ACTIVE INGREDIENT

    14%Azelaic Acid

  • PURPOSE

    Acne Cream

  • INDICATIONS & USAGE


    Clear Skin Solution
    Fade Acne Marks
    Soothing & Oil Control
    Apply proper amount to facial acne gently after morning and night cleansing, massage until absorbed.

  • WARNINGS

    For external use only.

  • WHEN USING

    Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

  • STOP USE

    Discontinue use if irritation occurs. If irritation persists, consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions: After cleaning your face, apply an appropriate amount of this product to your face and genty massage with your fingertips, focusing on the areas around the pimples until fully absorbed.

  • INACTIVE INGREDIENT

    Water, Propylene Glycol, Ethylhexyl Palmitate, Glycerin, Cetearyl Alcohol, Mineral Oil, Lauric/myristic/palmitic/stearic Glycerides, Glyceryl Stearate, Butylene Glycol, Totarol, Dimethicone, 0 -cymen-5-ol, PolyacrylamideC13-14 Isoparaffin, Laureth-7, Ceteareth-25, Beeswax, Hydroxyacetophenone, Allantoin, Carbomer, Triethanolamine, Xanthan Gum, Phenoxyethanol, Caprylhydroxamic Acid, Disodium Edta, Fragrance, Dipotassium Glycyrhizate, Centella Asiatica Extract, Scutellaria Baicalensis Root Extract, Polygonum Cuspidatum Root Extract, Camellia Sinensis Leaf Extract, Kanzou Ekisu, Chamomila Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf ExtractBacillus/soybean Ferment Extract, Folic Acid, 1,2-hexanediol, Sodium Hyaluronate, Jania Rubens Extract

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    BLOOMELLEE 14%GEL AZELAIC ACID CREAM 
    14%azelaic acid cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87386-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AZELAIC ACID (UNII: F2VW3D43YT) (AZELAIC ACID - UNII:F2VW3D43YT) AZELAIC ACID0.14 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)  
    CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)  
    POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    BACILLUS SUBTILIS STRAIN GB03 (UNII: 3X9V2CJ1MO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER (UNII: 0A5MM307FC)  
    ROSMARINUS OFFICINALIS (ROSEMARY) LEAF POWDER (UNII: IJ67X351P9)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CETEARETH-25 (UNII: 8FA93U5T67)  
    JANIA RUBENS WHOLE (UNII: ZQ94DKQ7LH)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    WATER (UNII: 059QF0KO0R)  
    TOTAROL (UNII: 67NH2854WW)  
    FRAGRANCE 13576 (UNII: 5EM498GW35)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    O-CYMEN-5-OL (UNII: H41B6Q1I9L)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)  
    BEESWAX (UNII: 2ZA36H0S2V)  
    TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
    LAURETH-7 (UNII: Z95S6G8201)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    GLYCYRRHIZA GLABRA WHOLE (UNII: M1F96IE0ZC)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    LAURIC/MYRISTIC/PALMITIC/STEARIC GLYCERIDES (UNII: 82TZ9D9546)  
    DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)  
    CHAMOMILE (UNII: FGL3685T2X)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    FOLIC ACID (UNII: 935E97BOY8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87386-002-011 in 1 BOX05/25/2026
    140 g in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/25/2026
    Labeler - Shenzhen Lanxi Trading Co., Ltd. (512086574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lanxi Trading Co., Ltd.512086574manufacture(87386-002)