Label: SNORESTOP NASOSPRAY 60- strychnos nux-vomica seed,atropa belladonna,ephedra distachya flowering twig,goldenseal,potassium dichromate,teucrium marum,histamine dihydrochloride liquid liquid

  • NDC Code(s): 61152-199-99
  • Packager: Green Pharmaceuticals Inc.
  • 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 June 16, 2022

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

  • Ingredients:

    Nux Vomica 4X,6X, Belladonna 6X, Ephedra 6X, Hydrastis canadensis 6X, Kali bich. 6X, Teucrium marum 6X, Histaminium 12X.

  • Base:

    Benzalkonium chloride, Glycerin, Potassium chloride, Potassium phospate, Purified water, Sodium chloride, Sodium phosphate.

  • Directions:

    Adults and children over 5 years old. Shake before each use. At bedtime, spray once into each nostril. Store below 30 degrees C.

  • Directions: Children over 5 years of age and Adults.

    Shake before use. 1. Remove cap and safety clip. 2. Prime by placing nozzle between first and second finger with thumb on the bottom of the bottle. Pump sprayer firmly and quickly until a fine spray appears. 3. Insert spray tip into one nostril, pointing the tip toward the back of the nose. Spray quickly while breathing in through your nose. Clean tip of nozzle after each use and replace cap. Store at room temperatur. May be used up to 4 times per day. Please discard 6 months after first use.

    For Maximum Results, use in conjunction with SnoreStop FastTabs or SnoreStop Extinguisher.

  • Warnings:

    Use only as directed. Keep this out of reach of children. Do not use on children under 5 years of age. If pregnant or breastfeeding, ask a physician before use. This product does not treat sleep apnea. For sleep apnea, consult with a specialist. If symptoms worsen after 14 days, discontinue use and ask a physician for help.

  • Comments or Questions?

    Toll free 1-877-SNOREST

    email: mal@snorestop.com

    Visit: www.snorestop.com

  • Keep out of reach of children.

    Keep out of reach of children.

  • Uses:

    Temporarily helps stop or reduce symptoms of non-apneic snoring. Individual results may vary.

  • NasoSpray 60

    NasoSpray60

  • INGREDIENTS AND APPEARANCE
    SNORESTOP NASOSPRAY 60 
    strychnos nux-vomica seed,atropa belladonna,ephedra distachya flowering twig,goldenseal,potassium dichromate,teucrium marum,histamine dihydrochloride liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61152-199
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED6 [hp_X]  in 9 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA6 [hp_X]  in 9 mL
    EPHEDRA DISTACHYA FLOWERING TWIG (UNII: R55VQ87DP3) (EPHEDRA DISTACHYA FLOWERING TWIG - UNII:R55VQ87DP3) EPHEDRA DISTACHYA FLOWERING TWIG6 [hp_X]  in 9 mL
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL6 [hp_X]  in 9 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE6 [hp_X]  in 9 mL
    TEUCRIUM MARUM (UNII: 10464S0TAA) (TEUCRIUM MARUM - UNII:10464S0TAA) TEUCRIUM MARUM6 [hp_X]  in 9 mL
    N.ALPHA.-METHYLHISTAMINE DIHYDROCHLORIDE (UNII: S6S98U0517) (HISTAMINE - UNII:820484N8I3) N.ALPHA.-METHYLHISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 9 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM (UNII: 7N6JUD5X6Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61152-199-999 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/19/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/18/2012
    Labeler - Green Pharmaceuticals Inc. (937749265)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    HomeoCare Laboratories, Inc.088248828manufacture(61152-199)
    Establishment
    NameAddressID/FEIBusiness Operations
    Green Pharmaceuticals Inc.937749265label(61152-199)
    Establishment
    NameAddressID/FEIBusiness Operations
    Coastal Contract Packaging137341611pack(61152-199)