Netimist by Neilmed Pharmaceuticals Inc. NetiMist - Adults

Netimist by

Drug Labeling and Warnings

Netimist by is a Homeopathic medication manufactured, distributed, or labeled by Neilmed Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NETIMIST- homeopathic sinus spray spray 
Neilmed Pharmaceuticals Inc.

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.

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NetiMist - Adults

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

Netimist Homeopathic Sinus Spray -Adults

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 homeopathic04/29/201602/03/2026
Labeler - Neilmed Pharmaceuticals Inc. (799295915)
Establishment
NameAddressID/FEIBusiness Operations
Neilmed Pharmaceuticals Inc.799295915manufacture(13709-234)

Revised: 2/2026
Document Id: 49e87db4-43e1-d854-e063-6294a90a60e2
Set id: af91e99e-2434-cef6-e053-2a95a90a38e6
Version: 4
Effective Time: 20260203