Label: SNORE DEFENSE (antimonium tartaricum, carbo vegetabilis, grindelia- robusta, lung suis, mucosa nasalis suis, nux vomica, sambucus nigra, sticta pulmonaria, teucrium marum 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 April 20, 2022

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

  • ACTIVE INGREDIENTS:

    (in each spray) 11.10% of Antimonium tartaricum 200C, Carbo vegetabilis 12X, Grindelia (Robusta) 200C, Lung suis 6X, Mucosa nasalis suis 6X, Nux vomica 12X, Sambucus nigra 3X, Sticta pulmonaria 200C, Teucrium marum 3X.

  • INDICATIONS:

    May help reduce the loudness and frequency of snoring and may promote a more restful night's sleep.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • WARNINGS:

    Persons who have symptoms of sleep apnea should consult a doctor.

    If pregnant or breast feeding, ask a doctor before use.

    Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

    Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS:

    Adults: Spray twice under the tongue 3 times per day, with last dose at bedtime and additional doses whenever sleep is interrupted.

  • INDICATIONS:

    May help reduce the loudness and frequency of snoring and may promote a more restful night's sleep.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • INACTIVE INGREDIENTS:

    Organic alcohol 20% v/v, Purified water.

  • QUESTIONS:

    DIST. BY LIDDELL LABORATORIES INC.

    WOODBINE, IA 51579

    WWW.LIDDELL.NET 1-800-460-7733

  • PACKAGE LABEL DISPLAY:

    ORAL SPRAYS

    LIDDELL

    LABORATORIES

    EST. 1994

    57 SN-

    Snore Defense

    HOMEOPATHIC

    1.0 FL. OZ. (30 ML)

    Snore Defense

  • INGREDIENTS AND APPEARANCE
    SNORE DEFENSE 
    antimonium tartaricum, carbo vegetabilis, grindelia (robusta), lung suis, mucosa nasalis suis, nux vomica, sambucus nigra, sticta pulmonaria, teucrium marum spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50845-0264
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5) ANTIMONY POTASSIUM TARTRATE200 [hp_C]  in 1 mL
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL12 [hp_X]  in 1 mL
    GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (GRINDELIA HIRSUTULA FLOWERING TOP - UNII:IDB0NAZ6AI) GRINDELIA HIRSUTULA FLOWERING TOP200 [hp_C]  in 1 mL
    SUS SCROFA LUNG (UNII: 7GL3G1COB3) (SUS SCROFA LUNG - UNII:7GL3G1COB3) SUS SCROFA LUNG6 [hp_X]  in 1 mL
    SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY) SUS SCROFA NASAL MUCOSA6 [hp_X]  in 1 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED12 [hp_X]  in 1 mL
    SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (SAMBUCUS NIGRA FLOWERING TOP - UNII:CT03BSA18U) SAMBUCUS NIGRA FLOWERING TOP3 [hp_X]  in 1 mL
    LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T) LOBARIA PULMONARIA200 [hp_C]  in 1 mL
    TEUCRIUM MARUM (UNII: 10464S0TAA) (TEUCRIUM MARUM - UNII:10464S0TAA) TEUCRIUM MARUM3 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50845-0264-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/10/202012/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/10/202012/17/2024
    Labeler - Liddell Laboratories (832264241)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(50845-0264) , api manufacture(50845-0264) , label(50845-0264) , pack(50845-0264)