Label: WILD YAM GINGER spray

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

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated March 19, 2024

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

View All Sections
  • INDICATIONS & USAGE

    Directions: ONLY FOR USE AS A NASAL SPRAY.

  • DOSAGE & ADMINISTRATION

    Use before bedtime. Ages 12 and older: 1-2 sprays. Ages 2-11: 1 spray. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredients: Dioscorea villosa (Wild yam) 2X, Zingiberis (Ginger) 2X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Sodium chloride, Grapefruit seed extract

    prepared using rhythmical processes

  • PURPOSE

    Use: Temporary relief of snoring.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.
    SHAKE WELL BEFORE USE.
    REFRIGERATE AFTER OPENING.
    USE WITHIN 30 DAYS OF OPENING.

  • QUESTIONS

    Questions? Call 866.642.2858
    Uriel, East Troy, WI 53120
    shopuriel.com Lot:

  • PRINCIPAL DISPLAY PANEL

    Wild yam Ginger Spray

  • INGREDIENTS AND APPEARANCE
    WILD YAM GINGER 
    wild yam ginger spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-9283
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIOSCOREA VILLOSA ROOT (UNII: IWY3IWX2G8) (DIOSCOREA VILLOSA ROOT - UNII:IWY3IWX2G8) DIOSCOREA VILLOSA ROOT2 [hp_X]  in 1 mL
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER2 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-9283-230 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc043471163manufacture(48951-9283)
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!