Resp Ease Liquid
FDA Label NDC 85379-113
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Venture Healthcare Ltd for the product Resp Ease (NDC 85379-113). 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 drug facts, active ingredient, purpose, uses:, warnings, • do not use, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Sodium Chloride 6%
Purpose
Moisturizer
Uses:
For dry nasal membranes
Warnings
NOT FOR INJECTION
Only use sealed vials do not use if vial is broken or already open
Keep out of reach of children
Do not use after expiration date
If you experience any adverse reaction discontinue use and call your physician
• Do Not Use
after expiration date
- Discontinue if you experience any adverse reaction and call your physician
Directions
If using with an OTC ear, nose, or throat device, then follow the directions provided with the device and only use as directed.
Inactive Ingredients
USP Water
Package Labelling:
Salin6 (Respease6)
5 mL NDC: 85379-113-11
* Please review the disclaimer below.
