US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 7, 2013 (13 years ago)

4 way Nasal Decongestant Menthol Nasal Spray, containing phenylephrine hydrochloride 1%…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.

What was recalled

4 way Nasal Decongestant Menthol Nasal Spray, containing phenylephrine hydrochloride 1%, a) 1/2-fl. oz. bottles (NDC 0067-2087-05) b) 1-fl. oz. bottles (NDC 0067-2087-01), OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.

Recalling firm
Novartis Consumer Health
NDC code
0067-2087-05
Origin
NE, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-210-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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