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  5. Label Information: Resp Ease

FDA Label for Resp Ease

View Indications, Usage & Precautions

Table of Contents

    1. DRUG FACTS
    2. ACTIVE INGREDIENT
    3. PURPOSE
    4. USES:
    5. WARNINGS
    6. •  DO NOT USE
    7. DIRECTIONS
    8. INACTIVE INGREDIENTS
    9. PACKAGE LABELLING:

Resp Ease Product Label

The following document was submitted to the FDA by the labeler of this product Laboratoire Unither. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Drug Facts




Active Ingredient



Sodium Chloride 3%


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:



5 mL NDC: 43014-1112-1


* Please review the disclaimer below.