Label: SINUS RELIEF- asafetida, echinacea angustifolia, calcium sulfide, potassium dichromate, luffa operculata whole, silicon dioxide, sinusitisinum pellet

  • NDC Code(s): 61727-335-21
  • Packager: Homeocare Laboratories
  • 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 31, 2018

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  • Active ingredients:

    Asafoetida 8X, Echinacea angustifolia 12X, Hepar sulph. 8X, Kali bic. 18X, Luffa operculata 9C, Silicea 10X, Sinusitisinum 18X.

  • Inactive ingredients:

    Sucrose/lactose.

  • Purpose:

    For the temporary relief of sinus pain and inflammation.

  • Warnings:

    If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.

  • Indications & Usage:

    Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

  • Dosage & Administration:

    Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

  • Keep out of reach of children.

    Keep out of reach of children.

  • Sinus Relief

    Sinus Relief

    Homeopathic Medicine

    85 Pellets

    SINUS-RELIEF.jpg

    sinus relief image

  • INGREDIENTS AND APPEARANCE
    SINUS RELIEF 
    asafetida, echinacea angustifolia, calcium sulfide, potassium dichromate, luffa operculata whole, silicon dioxide, sinusitisinum pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-335
    Route of AdministrationSUBLINGUAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASAFETIDA (UNII: W9FZA51AS1) (ASAFETIDA - UNII:W9FZA51AS1) ASAFETIDA8 [hp_X]  in 4 g
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA12 [hp_X]  in 4 g
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE8 [hp_X]  in 4 g
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE18 [hp_X]  in 4 g
    LUFFA OPERCULATA WHOLE (UNII: T013HM08S0) (LUFFA OPERCULATA WHOLE - UNII:T013HM08S0) LUFFA OPERCULATA WHOLE9 [hp_C]  in 4 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE10 [hp_X]  in 4 g
    SINUSITISINUM (UNII: B575563DM5) (SINUSITISINUM - UNII:B575563DM5) SINUSITISINUM18 [hp_X]  in 4 g
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-335-214 g in 1 TUBE; Type 0: Not a Combination Product07/24/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/24/2012
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-335)
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