• NasoClear® Day Formula

NasoClear® Day Formula

Nasal Spray - One Month Supply

SKU: 010

About The Product



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Our above-average solution helps support you when you need it the most, because it has six active natural ingredients to help keep you feeling better, and breathing better throughout the day.

It’s a natural water based nasal spray that helps open nasal passages for easy breathing and helps alleviate nasal congestion when the common cold, allergies or environmental pollutants start wearing you down. 


  • No drip, burning or stinging
  • No known side effects or rebound effects
  • Non-habit forming
  • Non-drowsy
  • No drug interactions
  • No contraindications

We’re pretty excited about NasoClear! So excited, that we will pay for your Domestic Shipping just to get you to try it!


Of course individual results may vary, so please tell us how well you think this works for you.

*Individual Results Vary 



Active Ingredients:

  • Ammonium carbonicum 3X: helps relieve nasal congestion 
  • Histaminum 12X: natural anti-histamine
  • Hydrastis 3X: helps dry out mucous
  • Melitotus 3X:helps relieve nasal congestion
  • Menthol 2X: helps open nasal passages
  • Sticta 3X: helps dry out mucous 

Inactive Ingredients:

  • Benzalkonium Chloride (0.04%)
  • Potassium Chloride
  • Purified water (98%)
  • Sodium Chloride
  • Sodium Phosphate
  • Potassium Phosphate
  • Benzyl Alcohol
  • Ethyl Alcohol


NasoClear Day Formula ingredients have been diluted out according to the Homeopathic Pharmacopeia of the United States. All ingredients are recognized as an official collection of accepted ingredients by the Federal Food, Drug and Cosmetic Act and are manufactured in FDA approved laboratories. Therefore this water based formula is harmless as it contains no alkaloids. Each ingredient derives from plant, mineral, or protein sources and is present only in harmless microscopic amounts in each dose. 

Dilution Scale: 6X is equal to one part per million.

Claims follow requirement in CPG 400.400 and GLP of Sections 502 & 503 of the FDCA (“The Act”) and Part 201 Title 21 of the CFR to include Principle Display Panel of OTC Drug Labeling under 21 CFR 201.62. Uses and claims are taken from various authorized Materia Medica for references. They have not been reviewed by the Federal Drug Administration.