Active Ingredient
Sodium Chloride 0.9%
Whisidom Saline Solution Liquid
FDA Label NDC 85248-178
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangxi Yudexi Pharmaceutical Co., Ltd for the product Whisidom Saline Solution (NDC 85248-178). 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 active ingredient, purpose, use, warnings, do not use, keep oot of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Moisturizer
Use
For dry nasal membranes
Warnings
·NOT FOR IN JECTIONS
·Only use sealed vialss. Do not use if vial is bioken or already open
Do Not Use
·Do not use after expiration date
·Discontinue you experience any adverse reaction and cal if your physician
Keep Oot Of Reach Of Children
Keep out of reach of children
Directions
·If using with an OTC ear, nose, or throat device, follow the directions provided with the device and only use as directed
Inactive Ingredients
USP Water
Principal Display Panel
0.9 (6816173509a72f931721caff0cd4760b)
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