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Resp Ease
sodium chloride · Resp Ease is an over-the-counter drug containing sodium chloride, made by 2 manufacturers.
- Type
- Over the counter
- Drug class
- Not classified
- Route
- Nasal
- Manufacturers
- 2
For dry nasal membranes
Related recalls
FDA drug recalls that name this drug or its active ingredient
- Class IIDrugOngoing10/07/2026Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for...Par Health USA, LLC · Crystallization
- Class IIDrugOngoing09/30/2026Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride...Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company · 2 products · Lack of Assurance of Sterility
- Class IIDrugOngoing09/30/2026Reliable -1 Laboratories, Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, Sterile, 0.5 FL OZ (15...Sterling Pharmaceutical Services LLC · Lack of Assurance of Sterility
- Class IDrugOngoing09/16/20260.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B....B BRAUN MEDICAL INC · Presence of Particulate Matter: particulate matter identified as...
- Class IIIDrugOngoing09/16/2026Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA...Ajanta Pharma USA Inc · Failed impurities/degradation specifications: (OOS) for Organic...
Active ingredients
Sodium Chloride 3% Purpose Moisturizer
Purpose
Moisturizer
Uses
For dry nasal membranes
Directions
If using with an OTC ear, nose, or throat device, then follow the directions provided with the device and only use as directed.
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
- Keep out of reach of children
- Do not use after expiration date Discontinue if you experience any adverse reaction and call your physician
Do not use
- Do not use after expiration date Discontinue if you experience any adverse reaction and call your physician
Keep out of reach of children
- Keep out of reach of children
Inactive ingredients
USP Water
Forms and strengths
From the FDA NDC Directory · 6 product codes
| Dosage form | Strength | Route | NDCs |
|---|---|---|---|
| Liquid | 30 mg/mL | nasal | 2 |
| Liquid | 60 mg/mL | nasal | 2 |
| Liquid | 70 mg/mL | nasal | 2 |
Side effect reports to FDA
FDA Adverse Event Reporting System (FAERS), 78,531 reports that list sodium chloride, data through 07/30/2026
Anyone can report a problem to FDA, and a report does not mean the drug caused the problem. Reports can be duplicated or incomplete, and counts depend on how widely a drug is used. Do not stop or change a medicine because of this list. Talk to your doctor or pharmacist.
Most often reported reactions
- Nausea5,628
- Myelosuppression5,180
- Dyspnea4,956
- Off label use4,929
- Headache4,496
- Pyrexia4,389
- Fatigue4,312
- Vomiting3,991
- Diarrhea3,852
- Pneumonia3,534
To report a side effect, use FDA MedWatch.
Manufacturers and labels
6 FDA labels
- Laboratoire UnitherShown hereLabel 03/16/2026 · NDC 43014-1112Full label
- Laboratoire UnitherLabel 03/16/2026 · NDC 43014-1114Full label
- Laboratoire UnitherLabel 03/16/2026 · NDC 43014-1113Full label
- Venture Healthcare LtdLabel 03/16/2026 · NDC 85379-113Full label
- Venture Healthcare LtdLabel 03/16/2026 · NDC 85379-114Full label
- Venture Healthcare LtdLabel 03/16/2026 · NDC 85379-112Full label
Resp Ease: common questions
- What is Resp Ease used for?
- For dry nasal membranes
- Is Resp Ease a prescription drug?
- No. Resp Ease is sold over the counter (OTC) without a prescription.
- Are there other products with the same active ingredient as Resp Ease?
- Yes. Other FDA-listed products with the same active ingredients include Sodium Chloride Normal Salt, Saline, Sodium Chloride, Sodium Chloride Hypertonicity.
- Who makes Resp Ease?
- 2 manufacturers list Resp Ease with the FDA, including Laboratoire Unither, Venture Healthcare Ltd.
Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 03/16/2026 · Label text is shown as published by the manufacturer. Not medical advice