Walgreens, NO DRIP Severe Anefrin Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour + Menthol, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7001-01, UPC 3 11917 18536 1.
Reported: October 24, 2018 Initiated: August 3, 2018 #D-0064-2019
Product Description
Walgreens, NO DRIP Severe Anefrin Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour + Menthol, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7001-01, UPC 3 11917 18536 1.
Reason for Recall
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Details
- Recalling Firm
- Product Quest Manufacturing LLC
- Units Affected
- 533,016 bottles
- Distribution
- Nationwide in the USA
- Location
- Daytona Beach, FL
Frequently Asked Questions
What product was recalled? ▼
Walgreens, NO DRIP Severe Anefrin Nasal Spray (Oxymetazoline HCl 0.05%) Nasal Decongestant, Maximum Strength, 12 Hour + Menthol, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7001-01, UPC 3 11917 18536 1.. Recalled by Product Quest Manufacturing LLC. Units affected: 533,016 bottles.
Why was this product recalled? ▼
CGMP Deviations: products manufactured under conditions that could impact its product quality.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 24, 2018. Severity: Moderate. Recall number: D-0064-2019.
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