Label: LANIMPRESS1%KETOCONAZOLEANTIDANDRUFFSHAMPOO lotion

  • NDC Code(s): 84372-041-01
  • Packager: Shenzhen Zhumeng Times Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 2, 2024

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

View All Sections
  • 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

    84372-041-02

  • INGREDIENTS AND APPEARANCE
    LANIMPRESS1%KETOCONAZOLEANTIDANDRUFFSHAMPOO 
    lanimpress1%ketoconazoleantidandruffshampoo lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84372-041
    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:84372-041-01125 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(84372-041)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!