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  2. Johnson & Johnson Recalls Sudafed Because of a Typo - AOL

    www.aol.com/news/2011-02-25-johnson-and-johnson...

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  3. Johnson & Johnson Recalls Sudafed Because of a Typo - AOL

    www.aol.com/2011/02/25/johnson-and-johnson...

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  4. Pseudoephedrine - Wikipedia

    en.wikipedia.org/wiki/Pseudoephedrine

    The drug reaches peak concentrations after 1 to 4 hours (mean 1.9 hours) in the case of the immediate-release formulation and after 2 to 6 hours in the case of the extended-release formulation. [1] [2] The onset of action of pseudoephedrine is 30 minutes. [1]

  5. FDA recall policies - Wikipedia

    en.wikipedia.org/wiki/FDA_recall_policies

    FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.

  6. Another Tylenol Recall, Plus Benadryl, Sudafed and Sinutab

    www.aol.com/2011/03/30/another-tylenol-recall...

    Johnson and Johnson's McNeil Consumer Healthcare recalled almost 800,000 bottles of Tylenol, Benadryl, Sudafed PE, and Sinutab products in two recalls linked to previous problems for the ...

  7. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]

  8. MedWatch - Wikipedia

    en.wikipedia.org/wiki/MedWatch

    In 2013, MedWatch introduced Form 3500B, which is designed to facilitate reporting by healthcare consumers. [4] The MedWatch system is intended to detect safety hazard signals for medical products. If a signal is detected, the FDA can issue medical product safety alerts or order product recalls, withdrawals, or labeling changes to protect the ...

  9. Rhinitis medicamentosa - Wikipedia

    en.wikipedia.org/wiki/Rhinitis_medicamentosa

    Rhinitis medicamentosa (or RM, also known as rebound congestion) is a condition of rebound nasal congestion suspected to be brought on by extended use of topical decongestants (e.g., oxymetazoline, phenylephrine, xylometazoline, and naphazoline nasal sprays) and certain oral medications (e.g., sympathomimetic amines and various 2-imidazolines) that constrict blood vessels in the lining of the ...