PlainRecalls
FDA Drug Low Class III Terminated

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.

Reported: March 27, 2013 Initiated: March 7, 2013 #D-210-2013

Product Description

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.

Reason for Recall

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

Details

Recalling Firm
Novartis Consumer Health
Units Affected
44,604/ .5-fl. oz. bottles and 439,452 /1-fl. oz. bottles
Distribution
Nationwide and Panama
Location
Lincoln, NE

Frequently Asked Questions

What product 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.. Recalled by Novartis Consumer Health. Units affected: 44,604/ .5-fl. oz. bottles and 439,452 /1-fl. oz. bottles.
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or expiration date may be illegible.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 27, 2013. Severity: Low. Recall number: D-210-2013.