Label: HABEN HERB F CAP- acetaminophen, dried cinnamon extract capsule

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated September 8, 2024

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  • ACTIVE INGREDIENT

    Acetaminophen, Dried cinnamon Extract

  • PURPOSE

    Relieve your cold symptoms

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    • 15 years old and older and adults: 2 capsules once

    • 7 years old and older and under 15 years old: 1 capsule once

    • Take 3 times a day, 30 minutes after meals

  • WARNINGS

    Warnings

    For external use only.

    Do not use in the eyes by putting this product into the rectum by using fingers or any mechanical device or applicator.

    Ask a doctor before use if you have a vaginal discharge, rectal bleeding, diaper rash.

    When using this product consult a doctor before exceeding recommended dosage.

    Stop use and ask a doctor if condition gets worse, condition persists for more than 7 days, condition clears up and occurs again with within a few days. Do not begin to use any other hydrocortisone product unless you have consulted a doctor.

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

  • INACTIVE INGREDIENT

    Dried licorice Extract,Ribo flavin,Guaifenesin,

    Dried platycodon root Extract with 50% Ethanol

  • DOSAGE & ADMINISTRATION

    for topical use

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    HABEN HERB F CAP 
    acetaminophen, dried cinnamon extract capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72988-0040
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CINNAMON (UNII: 5S29HWU6QB) (CINNAMON - UNII:5S29HWU6QB) CINNAMON10 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    GUAIFENESIN (UNII: 495W7451VQ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeCAPSULESize19mm
    FlavorImprint Code HabenHerbF
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72988-0040-110 in 1 PACKAGE; Type 0: Not a Combination Product09/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/01/2024
    Labeler - Lydia Co., Ltd. (695735569)
    Registrant - Lydia Co., Ltd. (695735569)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lydia Co., Ltd.695735569manufacture(72988-0040)