Label: NETIMIST- homeopathic sinus spray spray

  • NDC Code(s): 13709-234-02
  • Packager: Neilmed Pharmaceuticals Inc.
  • Category: HUMAN OTC DRUG LABEL

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 11, 2024

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  • Directions

    • Suitable for children over 6 with proper adult supervision.
    • For children 6 and under, consult a physician before use.
    • Shake well.
    • Remove cap & safety clip.
    • Hold with thumb at bottom of bottle & nozzle between fingers.
    • Prime pump prior to initial use by depressing several times.
    • Insert tip of nozzle, just past the nasal opening (1/8th - 1/4th inch)
    • Pump once inside each nostril & gently inhale.
    • Wait at least 30 seconds or longer before blowing nose.
    • Use as needed every 2-4 hours & in crowded public environments such as schools, public transportation.
  • Warnings

    • For Intransal use only.
    • Use only as directed.
  • Inactive Ingredients

    Aloe vera, deionized water, erythritol, essential oils of mandarin and ginger, grapefruit seed extract, polysorbate 20 (vegetable source), sodium chloride (USP) and sodium bicarbonate (USP) (added for ph adjustment)

  • Uses

    For temporary relief of :

    • Nasal congestion
    • Inflammation of mucous membranes
    • Thick mucus & phlegm
  • Keep out of reach of children

    Suitable for children over 6 with proper adult supervision.

  • Drug Facts

    Active Ingredient : Kali Muriaticum 6X

    Purpose: Upper respiratory mucus & congestion

  • Drug Facts

    Active Ingredient : Kali Muriaticum 6X

  • PRINCIPAL DISPLAY PANEL

    Netimist Homeopathic Sinus Spray -Adults

  • INGREDIENTS AND APPEARANCE
    NETIMIST 
    homeopathic sinus spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13709-234
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE6 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    GINGER OIL (UNII: SAS9Z1SVUK)  
    MANDARIN OIL (UNII: NJO720F72R)  
    GRAPEFRUIT SEED OIL (UNII: 598D944HOL)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    ERYTHRITOL (UNII: RA96B954X6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13709-234-021 in 1 BOX04/29/2016
    11 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/29/2016
    Labeler - Neilmed Pharmaceuticals Inc. (799295915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Neilmed Pharmaceuticals Inc.799295915manufacture(13709-234)
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