Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated Dec 28, 2023 (3 years ago)

Nasal Spray Original No Drip Oxymetazoline HCl Nasal Solution (Oxymetazoline Hydrochloride)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

Nasal Spray Original No Drip Oxymetazoline HCl Nasal Solution, 12 Hour Pump Mist, 1 FL oz. (30 mL) bottle, a) Quality Choice, Distributed by C.D.M.A. Inc., 43157 W 9 Mile Rd, Novi, MI 48375, NDC# 63868-607-01, UPC 6-35515-98843-9, b) Premier Value, Distributed by: Pharmacy Value Alliance, LLC, 407 East Lancaster Avenue, Wayne, PA 19087 UPC 8-40986-03509-8.

Affected NDC 63868-0607-01

Compare with the code on your package — it is the most precise check available.

Drug: Oxymetazoline Category: Allergy & Cold Medication

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Oxymetazoline Hydrochloride
NDC 63868-0607
.05 g/100mL Spray
Nasal
Chain Drug Marketing Association INC. OTC
Recalling firm
Seaway Pharma Inc.
NDC code
63868-607-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0214-2024 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Oxymetazoline recalls

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Class III · Low risk

SinuFrin Decongestant

Sub-potent Drug

Ongoing Other Neilmed Pharmaceuticals Inc NDC 13709-325-01 D-0569-2024

Other recalls by Seaway Pharma Inc.

All 2023 recalls
Class II · Moderate risk

Premier Value Tussin Cough DM

CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.

Ongoing Microbial contamination Seaway Pharma Inc. D-0215-2024