Label: LANIMPRESS1%KETOCONAZOLEANTIDANDRUFFSHAMPOO lotion

  • NDC Code(s): 84372-042-01
  • Packager: Shenzhen Zhumeng Times Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 2, 2024

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  • Active ingredients

    Ketoconazole 1% Anti-dandruff shampoo

  • Purpose

    controls flaking, scaling and itching associated with dandruff

  • Uses

    wet hair thoroughly

    apply shampoo, generously lather,rinse thoroughiy. Repeat

    use every 3-4 days for up to 8 weeks or as directed by a doctor. Then use oniy as needed to controt dandruff

  • Warnings

    For external use only

    Do not use

    on scalp that is broken or inflamed

    if you are allergic to ingredients in this product

  • Dosage and administration

    For external use only.

  • Do not use

    Stop use and ask a doctor if rash occurs

  • When using section

    rash appears

    condition worsens or does not improve in 2-4 weeks.

  • stop use

    Do not use

    on scalp that is broken or inflamed

    if you are allergic to ingredients in this product

  • Keep out of reach of children

    Keep out of reach of children.lf swallowed, get medical help or contacta Poison Control Center right away.

  • Inactive ingredients

    benzyl alcohol, BHT, blue 1, citric acid,cocamide MEA, fragrance, glycol distearate, hydrochloricacid, hydroxypropyl methylcellulose, polyquaternium-7, sodium chioride, sodium cocoyi sarcosinate, sodium hydroxide, sodiumlaureth sulfate, tetrasodium EDTA, waterCAPRYLATE,CARBOMER,METHYLPARABEN,TRIETHANOLAMINE,SODIUM HYALURONATE,DISODIUM EDTA，water

  • PRINCIPAL DISPLAY PANEL

    84372-042-02

  • INGREDIENTS AND APPEARANCE
    LANIMPRESS1%KETOCONAZOLEANTIDANDRUFFSHAMPOO 
    lanimpress1%ketoconazoleantidandruffshampoo lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84372-042
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE5 g  in 125 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    WATER (UNII: 059QF0KO0R)  
    IVERMECTIN (UNII: 8883YP2R6D)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    8-PENTADECANONE (UNII: QO7H8D8OSB)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ACONITIC ACID (UNII: 93371T1BXP)  
    FRAGRANCE 13576 (UNII: 5EM498GW35)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84372-042-01125 mL in 1 BOX; Type 0: Not a Combination Product09/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01609/02/2024
    Labeler - Shenzhen Zhumeng Times Technology Co., Ltd. (631852731)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Zhumeng Times Technology Co., Ltd.631852731manufacture(84372-042)
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