Label: SSANGGI TANG- ssanghwa extract liquid

  • 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 October 19, 2019

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

View All Sections
  • ACTIVE INGREDIENT

    ssanghwa extract (peony root, rehmannia root, cnidium rhizome, astragalus root, angelica gias root, cinnamon bark, licorice, raw ginger, jujube)

  • PURPOSE

    for cure fatigue, physical weakness, and illness such as cold sweats

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    take 1 pouch 3 times a day

  • WARNINGS

    do not intake if the product is found to have expired or corrupted

    when using this product be aware that the contents may flow when opening

    stop use and ask a doctor if you have certain body types and allergies, it can cause a severe allergic reaction

  • INACTIVE INGREDIENT

    water, liquid fructose

  • DOSAGE & ADMINISTRATION

    For oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SSANGGI TANG 
    ssanghwa extract liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72988-0022
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P) (PAEONIA LACTIFLORA ROOT - UNII:3Z3866YW6P) PAEONIA LACTIFLORA ROOT0.9785 g  in 100 mL
    REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (REHMANNIA GLUTINOSA ROOT - UNII:1BEM3U6LQQ) REHMANNIA GLUTINOSA ROOT0.6745 g  in 100 mL
    LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97) (LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT - UNII:RR83T99U97) LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT0.627 g  in 100 mL
    ASTRAGALUS GUMMIFER ROOT (UNII: 10T15Y9F0M) (ASTRAGALUS GUMMIFER ROOT - UNII:10T15Y9F0M) ASTRAGALUS GUMMIFER ROOT0.4845 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FRUCTOSE (UNII: 6YSS42VSEV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72988-0022-180 mL in 1 POUCH; Type 0: Not a Combination Product10/08/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/08/2019
    Labeler - LYDIA Co., Ltd (695735569)
    Registrant - LYDIA Co., Ltd (695735569)
    Establishment
    NameAddressID/FEIBusiness Operations
    I World Pharmaceutical Co., Ltd688222857manufacture(72988-0022)
    Establishment
    NameAddressID/FEIBusiness Operations
    LYDIA Co., Ltd695735569label(72988-0022)
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!