Label: 1912 HERB CO VITAL AIR HERB- honeysuckle, bellflower, ginseng powder

  • NDC Code(s): 83933-0001-1
  • Packager: Agricultural Corporation YUBIMUHUAN CO Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 January 2, 2024

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  • ACTIVE INGREDIENT

    Honeysuckle(20%), Bellflower(15%) Ginseng(5%)

  • INACTIVE INGREDIENT

    Burdock(5%), Mint(5%), Lilyturf(5%), Goji Berry(5%), Heartleaf(5%), Schisandra Berry(5%), Ginger(5%), Green Tea(5%), Prickly ash(5%), Dried Tangerine Peel(5%), Perilla Leaf(5%), Barley Flour(5%)

  • PURPOSE

    relief of allergic rhinitis, improvement of bronchial function, cough relief

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Take 1 pouch (3g) three time a day after a meal

  • WARNINGS

    If you have an unusual or allergic constitution, check the ingredients before consuming.

  • DOSAGE & ADMINISTRATION

    for oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    1912 HERB CO VITAL AIR HERB 
    honeysuckle, bellflower, ginseng powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83933-0001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) (LONICERA CAPRIFOLIUM FLOWER - UNII:5N1WD9784U) LONICERA CAPRIFOLIUM FLOWER20 g  in 100 g
    PLATYCODON GRANDIFLORUS WHOLE (UNII: WC73QE9274) (PLATYCODON GRANDIFLORUS WHOLE - UNII:WC73QE9274) PLATYCODON GRANDIFLORUS WHOLE15 g  in 100 g
    PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0) (PANAX GINSENG ROOT OIL - UNII:P9T4K47OM0) PANAX GINSENG ROOT OIL5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    MINT (UNII: FV98Z8GITP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83933-0001-13 g in 1 POUCH; Type 0: Not a Combination Product01/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/03/2024
    Labeler - Agricultural Corporation YUBIMUHUAN CO Ltd (695152747)
    Registrant - Agricultural Corporation YUBIMUHUAN CO Ltd (695152747)
    Establishment
    NameAddressID/FEIBusiness Operations
    Agricultural Corporation YUBIMUHUAN CO Ltd695152747manufacture(83933-0001)