Label: EQUIOPATHICS NOSE AND SINUS- hepar sulphuris calcareum, kali bichromicum, natrum muriaticum, phosporus, petroleum liquid

  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 3, 2020

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

  • EquioPathics Nose Relief

    Provides support for a healthy nasal and sinus tract

    RED WET EYES-SNEEZING-NASAL DISCHARGE

  • DIRECTIONS FOR USE AND DOSAGE

    Dose remedy directly into mouth, in water or at meal time. Acute: 1 dose every 15 minutes for one hour. Chronic: 1 dose twice daily. Reduce dosing frequency with improvement.

     animal to be treated cattle, houses and donkeysgoats and sheep
     mL per dose 2 mL 1 mL

  • INDICATIONS

    Provides support for a healthy nasal and sinus tract. Can aid with a runny nose, watery eyes, sneezing and congestion.

  • Ingredients HPUS: ACTIVE

    Hepar sulphuris calcareum 6c, 30c, Kali Bichromicum 6c, 30c, Natrum muriaticum 6c, 30c, Phosphorus 6c, 30c, Petroleum 6c, 30c

  • Inactive Ingredients

    USP Alcohol, Purified water

  • Contact Veterinarian

    Contact your veterinarian if problems persist.

    Visit homeopet.com for detailed dosing and further information.

  • EQ Nose Relief label

    Product label

  • INGREDIENTS AND APPEARANCE
    EQUIOPATHICS NOSE AND SINUS 
    hepar sulphuris calcareum, kali bichromicum, natrum muriaticum, phosporus, petroleum liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:61571-446
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE6 [hp_C]  in 120 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE6 [hp_C]  in 120 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6 [hp_C]  in 120 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS6 [hp_C]  in 120 mL
    PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM6 [hp_C]  in 120 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61571-446-04120 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/15/1995
    Labeler - HomeoPet, LLC (121272657)
    Registrant - HomeoPet, LLC (121272657)
    Establishment
    NameAddressID/FEIBusiness Operations
    Speciality Pharma Manufacturing LLC013957125api manufacture, manufacture