Active Ingredient
Sodium Chloride 0.9%
Whisidom Saline Solution Liquid
FDA Label NDC 85248-178
9 label sections · Submitted to the FDA by Jiangxi Yudexi Pharmaceutical Co., Ltd · 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 out 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
Daily Personal Care
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 use if you experience any adverse reaction and call your physician.
Keep Out Of Reach Of Children
Keep out of reach of children
Directions
Hold the ampoule gently and twist the top. Squeeze the ampoule to dispense the saline. Discard after use.
Inactive Ingredients
USP Water
Principal Display Panel
0.9 (364b50e9f49143409a3ec85eefe95b83)
* Please review the disclaimer below.
