Label: ALLERGY RELIEF- allium cepa, apis mellifica, aralia racemosa, blatta orientalis, euphrasia officinalis, galphimia glauca, hedera helix, luffa operculata, okoubaka, sabadilla. 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 21, 2015

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS (HPUS*):

    Allium Cepa 5X, Apis Mellifica 5X, Aralia Racemosa 5X, Euphrasia Officinalis 5X, Galphimia Glauca 5X, Hedera Helix 5X, Luffa Operculata 5X, Okoubaka 5X, Sabadilla 5X.

    * The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States.


  • INDICATIONS & USAGE

    USES: Temporarily relieves respiratory symptoms caused by common allergens.


  • WARNINGS

    WARNINGS:

    If pregnant or breast-feeding, ask a health professional before use. If symptoms persist for more than a week, discontinue use and contact a health care professional.

    Keep out of the reach of children.


  • DOSAGE & ADMINISTRATION

    DIRECTIONS:

    Shake 10 times before use. Adults and children above 12 years of age: spray 3-4 times under the tongue every 15 minutes, extend interval as symptoms improve or as directed by a health care professional. Children under 12: use half the adult dose.


  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:

    Ethanol Alcohol 16%, Glycerin, Purified Water.


  • QUESTIONS

    Mfg. By: OHM PHARMA INC.

    Mineral Wells, TX 76067


  • OTHER SAFETY INFORMATION

    Pharmaceutical Grade

    Professional Use Only

    Product of USA

  • PURPOSE

    Allergy Relief


  • PRINCIPAL DISPLAY PANEL

    HOMEOPATHIC MEDICINE

    NDC: 66096-158-05

    ALLERGY RELIEF

    Natural - Safe - Effective

    No Side Effects

    2 fl oz (59 mL) / 16% Alcohol

    2oz bottle label

  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF  
    allium cepa, apis mellifica, aralia racemosa, blatta orientalis, euphrasia officinalis, galphimia glauca, hedera helix, luffa operculata, okoubaka, sabadilla. spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-158
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION5 [hp_X]  in 1 mL
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA5 [hp_X]  in 1 mL
    ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU) ARALIA RACEMOSA ROOT5 [hp_X]  in 1 mL
    BLATTA ORIENTALIS (UNII: 535787266D) (BLATTA ORIENTALIS - UNII:535787266D) BLATTA ORIENTALIS5 [hp_X]  in 1 mL
    EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA5 [hp_X]  in 1 mL
    GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E) GALPHIMIA GLAUCA FLOWERING TOP5 [hp_X]  in 1 mL
    HEDERA HELIX FLOWERING TWIG (UNII: 3D10KUA6BM) (HEDERA HELIX FLOWERING TWIG - UNII:3D10KUA6BM) HEDERA HELIX FLOWERING TWIG5 [hp_X]  in 1 mL
    LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU) LUFFA OPERCULATA FRUIT5 [hp_X]  in 1 mL
    OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (OKOUBAKA AUBREVILLEI BARK - UNII:MK2074187Z) OKOUBAKA AUBREVILLEI BARK5 [hp_X]  in 1 mL
    SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED5 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66096-158-0559 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/17/2015
    Labeler - OHM PHARMA INC. (030572478)
    Registrant - OHM PHARMA INC. (030572478)
    Establishment
    NameAddressID/FEIBusiness Operations
    OHM PHARMA INC.030572478manufacture(66096-158)