Label: ALLERGICLEAR-M- adrenalinum, calcarea fluorica, calcarea phosphorica, euphrasia officinalis, histaminum hydrochloricum, kali muriaticum, natrum muriaticum, silicea 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 December 26, 2023

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

  • HPUS Active Ingredient

    HPUS Active Ingredients: Each dose contains equal parts of: Adrenalinum 7C, Calcarea fluorica 8X, Calcarea phosphorica 8X, Euphrasia officinalis 4X, Histaminum hydrochloricum 7C, Kali muriaticum 8X, Natrum muriaticum 8X, Silicea 8X.

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

  • Uses*

    Uses*: Homeopathic medicine for the temporary relief of allergy and hay fever symptoms.

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

  • Warnings

    Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    Directions: For all ages: Mix 0.50 mL in 1/4 cup of water and silp slowly. Repeat 3-5 times daily. For acute symptoms, repeat every 30 minutes as needed until symptoms subside, or up to 48 hours. If preferred, drops may be taken directly in the mouth.

  • OTHER SAFETY INFORMATION

    Contains no artificial flavors or colorants. No gluten added.

    Tamper resistant for your protection. Use only if safety seal is intact.

  • Inactive Ingredients

    Inactive Ingredients: Purified water, USP grain alcohol (20% by volume).

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medication out of reach of children.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • PURPOSE

    Relieves allergy symptoms

  • PRINCIPAL DISPLAY PANEL

    AllergiClear M

  • INGREDIENTS AND APPEARANCE
    ALLERGICLEAR-M 
    adrenalinum, calcarea fluorica, calcarea phosphorica, euphrasia officinalis, histaminum hydrochloricum, kali muriaticum, natrum muriaticum, silicea liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68703-341
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM PHOSPHATE8 [hp_X]  in 59 mL
    CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O) CALCIUM FLUORIDE8 [hp_X]  in 59 mL
    EUPHRASIA OFFICINALIS LEAF (UNII: L4W0HL3P0F) (EUPHRASIA OFFICINALIS LEAF - UNII:L4W0HL3P0F) EUPHRASIA OFFICINALIS LEAF4 [hp_X]  in 59 mL
    EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE7 [hp_C]  in 59 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE7 [hp_C]  in 59 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE8 [hp_X]  in 59 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE8 [hp_X]  in 59 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION8 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68703-341-0259 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product10/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/01/2019
    Labeler - Silver Star Brands (006070379)
    Registrant - Silver Star Brands (006070379)
    Establishment
    NameAddressID/FEIBusiness Operations
    OHM Pharma030572478manufacture(68703-341)