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

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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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)
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