Otc - Active Ingredient
Active ingredient: xanthan gum
Nosno
FDA Label NDC 52345-5001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by K&j.c Co., Ltd for the product Nosno (NDC 52345-5001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive ingredient: sodium hyaluronate, propolis, polysorbate, L-menthol, methyl p-hydroxybenzoate, purified water
Otc - Purpose
Reduce and prevent noisy snoring
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Tilt your head back and spray into each nose as 3~4 timesbreathe deeply to be absorbed into each nose easily
Warnings
Discard when passed 6 weeks after open
Dosage & Administration
Nasal use only
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