Label: ALLERGY MIX LOS ANGELES- local remedy los angeles liquid

  • 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 January 31, 2019

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

View All Sections
  • DRUG FACTS

  • ACTIVE INGREDIENT

    Active Ingredients
    Alternaria Tenuis 6X, Cladosporium Fulvum 6X, European
    Olive 6X, Fruitless Mulberry 6X, Mountain Cedar 6X,
    Oleander 6X, Rocky Mountain Juniper 6X, Ustilago Smut 6X
    Histaminum Hydrochloricum 12X, Sabadilla 12X, Ragweed 12X

  • PURPOSE

    Purpose
    Allergy symptom relief

  • INDICATIONS & USAGE

    Uses: Allergy symptom relief
    For temporary relief of symptoms due to hay fever or other
    respiratory allergies. Runny nose, sneezing, irritated eyes,
    nasal congestion, itchy nose and throat, sinus pain.

  • WARNINGS

    Warnings
    Children under 12 years of age: consult a physician.
    If pregnant or breastfeeding, ask a health care professional
    before use. If symptoms persist or worsen consult a
    physician.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • DOSAGE & ADMINISTRATION

    Directions
    Adults & children 12 years of age and older: 10-15 drops
    under tongue, up to 6 times daily, or as directed by a health
    care professional. Avoid food and fluids 15 minutes before
    and after each use.

  • INACTIVE INGREDIENT

    Inactive Ingredients
    20% USP Ethanol, USP Purified Water.

  • Principal Display Package

       ALLERGY MIX™
    – LOCAL REMEDY –
         Los Angeles

    ALLERGY RELIEF

    RUNNY NOSE, SNEEZING,
    IRRITATED EYES, SINUS
    CONGESTION & MORE

    NO SIDE EFFECTS

    HOMEOPATHIC MEDICINE

    NET WT. 1 FL. OZ. (29.6 ML)

    NDC# 72617-2003-1

    Manufactured for: American Standard Nutraceuticals
    Las Vegas, Nevada 89120, allergymix.com 800-959-3796

    1  81163 00011  0

    LOT # XXXX

    LA AlrgyMix Liquid 2003-1

    res

  • INGREDIENTS AND APPEARANCE
    ALLERGY MIX LOS ANGELES 
    local remedy los angeles liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72617-2003
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (ALTERNARIA ALTERNATA - UNII:52B29REC7H) ALTERNARIA ALTERNATA6 [hp_X]  in 29.6 mL
    PASSALORA FULVA (UNII: HR6H5057CO) (PASSALORA FULVA - UNII:HR6H5057CO) PASSALORA FULVA6 [hp_X]  in 29.6 mL
    OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (OLEA EUROPAEA FLOWER - UNII:498M34P1VZ) OLEA EUROPAEA FLOWER6 [hp_X]  in 29.6 mL
    WHITE MULBERRY (UNII: MN25R0HH5A) (WHITE MULBERRY - UNII:MN25R0HH5A) WHITE MULBERRY6 [hp_X]  in 29.6 mL
    JUNIPERUS ASHEI POLLEN (UNII: 544F8MEY0Y) (JUNIPERUS ASHEI POLLEN - UNII:544F8MEY0Y) JUNIPERUS ASHEI POLLEN6 [hp_X]  in 29.6 mL
    NERIUM OLEANDER FLOWER (UNII: WO4WVF1WVM) (NERIUM OLEANDER FLOWER - UNII:WO4WVF1WVM) NERIUM OLEANDER FLOWER6 [hp_X]  in 29.6 mL
    JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (JUNIPERUS SCOPULORUM POLLEN - UNII:0G82TT8ZFY) JUNIPERUS SCOPULORUM POLLEN6 [hp_X]  in 29.6 mL
    USTILAGO MAYDIS (UNII: 4K7Z7K7SWG) (USTILAGO MAYDIS - UNII:4K7Z7K7SWG) USTILAGO MAYDIS6 [hp_X]  in 29.6 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 29.6 mL
    SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED12 [hp_X]  in 29.6 mL
    AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA12 [hp_X]  in 29.6 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72617-2003-129.6 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/23/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/23/2019
    Labeler - ASN (012050067)
    Registrant - ASN (012050067)
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!