Inactive Ingredient
Inactive Ingredients
None
Saline Wash
FDA Label NDC 11673-408
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Saline Wash (NDC 11673-408). 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 inactive ingredient, otc - active ingredient, warnings, otc - purpose, otc - keep out of reach of children, indications & usage, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredients
(in each packet)
Sodium Bicarbonate USP 700 mg
Sodium Chloride USP 1200 mg
Warnings
Warnings
For external use only
Otc - Purpose
Purpose
Nasal wash
Otc - Keep Out Of Reach Of Children
Keep out of reach from children
Indications & Usage
Uses
Temporarily relieves symptoms associated with sinusitis, colds, flu or allergies
Sneezing
Runny nose
Nasal stuffiness
Post nasal drip
Removes inhaled irritants (dust, pollen)
Promotes nasal and sinus drainage
Helps reduce swelling of nasal membranes
Dosage & Administration
Directions
Adults and children 4 years and over: 1-2 packets every 2 hours as needed
Children under 4 years: Consult a doctor
Consult Instructions for Use for proper use
Other Safety Information
Other Information
Inspect saline solution packets for integrity
Do not use if open or torn
Protect saline solution packets from excessive heat and moisture
Package Label.Principal Display Panel
Copy Of Label (Ascent Targetlabel)
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