Hand Wash

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Hand Wash Recall

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Side Effects & Adverse Reactions

For external use only-hands only

irritation or redness develops
condition persists for more than 72 hours

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Legal Issues

There is currently no legal information available for this drug.

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FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

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Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

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FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

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Uses

for handwashing to decrease bacteria on the skin

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History

There is currently no drug history available for this drug.

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Other Information

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Sources

Hand Wash Manufacturers

Better Living Brands Llc

Hand Wash | Better Living Brands Llc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Uline

Hand Wash | Uline

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Winco Foods, Llc

Hand Wash | Winco Foods, Llc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Demoulas Super Markets, Inc

Hand Wash | Demoulas Super Markets, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Publix Super Markets

Hand Wash | Publix Super Markets

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Dza Brands, Llc

Hand Wash | Dza Brands, Llc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Fred’s Inc

Hand Wash | Fred's Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Harmon Stores, Inc

Hand Wash | Harmon Stores, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Supervalu Inc

Hand Wash | Supervalu Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Supervalu Inc

Hand Wash | Supervalu Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Supervalu Inc.

Hand Wash | Supervalu Inc.

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Wakefern Food Corp

Hand Wash | Wakefern Food Corp

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Wakefern Food Corp

Hand Wash | Wakefern Food Corp

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Valu Merchandisers, Co

Hand Wash | Valu Merchandisers, Co

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
American Sales

Hand Wash | American Sales

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Meijer Distribution, Inc

Hand Wash | Meijer Distribution, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Target Corporation

Hand Wash | Target Corporation

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Target Corporation

Hand Wash | Target Corporation

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Valu Merchandisers, Co

Hand Wash | Valu Merchandisers, Co

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Harmon Stores, Inc

Hand Wash | Harmon Stores, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Wakefern Food Corp

Hand Wash | Wakefern Food Corp

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
The Kroger Co

Hand Wash | The Kroger Co

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Onpoint, Inc

Hand Wash | Onpoint, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Onpoint, Inc

Hand Wash | Onpoint, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Your Military Exchange

Hand Wash | Your Military Exchange

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Demoulas Super Markets, Inc

Hand Wash | Demoulas Super Markets, Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Salado Sales, Inc

Hand Wash | Proficient Rx Lp

Initial Treatment
The recommended starting dose for mirtazapine tablets USP is 15 mg/day, administered in a single dose, preferably in the evening prior to sleep. In the controlled clinical trials establishing the efficacy of mirtazapine tablets USP in the treatment of major depressive disorder, the effective dose range was generally 15 to 45 mg/day. While the relationship between dose and satisfactory response in the treatment of major depressive disorder for mirtazapine tablets USP has not been adequately explored, patients not responding to the initial 15 mg dose may benefit from dose increases up to a maximum of 45 mg/day. Mirtazapine tablets USP have an elimination half-life of approximately 20 to 40 hours; therefore, dose changes should not be made at intervals of less than 1 to 2 weeks in order to allow sufficient time for evaluation of the therapeutic response to a given dose.
Elderly and Patients With Renal or Hepatic Impairment
The clearance of mirtazapine is reduced in elderly patients and in patients with moderate to severe renal or hepatic impairment. Consequently, the prescriber should be aware that plasma mirtazapine levels may be increased in these patient groups, compared to levels observed in younger adults without renal or hepatic impairment (see PRECAUTIONS and CLINICAL PHARMACOLOGY).
Maintenance/Extended Treatment
It is generally agreed that acute episodes of depression require several months or longer of sustained pharmacological therapy beyond response to the acute episode. Systematic evaluation of mirtazapine tablets USP has demonstrated that its efficacy in major depressive disorder is maintained for periods of up to 40 weeks following 8 to 12 weeks of initial treatment at a dose of 15 to 45 mg/day (see CLINICAL PHARMACOLOGY). Based on these limited data, it is unknown whether or not the dose of mirtazapine tablets USP needed for maintenance treatment is identical to the dose needed to achieve an initial response. Patients should be periodically reassessed to determine the need for maintenance treatment and the appropriate dose for such treatment.
Switching a Patient To or From a Monoamine Oxidase Inhibitor (MAOI) Intended to Treat Psychiatric Disorders
At least 14 days should elapse between discontinuation of an MAOI intended to treat psychiatric disorders and initiation of therapy with mirtazapine tablets USP. Conversely, at least 14 days should be allowed after stopping mirtazapine tablets USP before starting an MAOI intended to treat psychiatric disorders (see CONTRAINDICATIONS).
Use of Mirtazapine Tablets USP With Other MAOIs, Such as Linezolid or Methylene Blue
Do not start mirtazapine tablets USP in a patient who is being treated with linezolid or intravenous methylene blue because there is an increased risk of serotonin syndrome. In a patient who requires more urgent treatment of a psychiatric condition, other interventions, including hospitalization, should be considered (see CONTRAINDICATIONS).

In some cases, a patient already receiving therapy with mirtazapine tablets USP may require urgent treatment with linezolid or intravenous methylene blue. If acceptable alternatives to linezolid or intravenous methylene blue treatment are not available and the potential benefits of linezolid or intravenous methylene blue treatment are judged to outweigh the risks of serotonin syndrome in a particular patient, mirtazapine tablets USP should be stopped promptly, and linezolid or intravenous methylene blue can be administered. The patient should be monitored for symptoms of serotonin syndrome for 2 weeks or until 24 hours after the last dose of linezolid or intravenous methylene blue, whichever comes first. Therapy with mirtazapine tablets USP may be resumed 24 hours after the last dose of linezolid or intravenous methylene blue (see WARNINGS).

The risk of administering methylene blue by non-intravenous routes (such as oral tablets or by local injection) or in intravenous doses much lower than 1 mg/kg with mirtazapine tablets USP is unclear. The clinician should, nevertheless, be aware of the possibility of emergent symptoms of serotonin syndrome with such use (see WARNINGS).
Discontinuation of Mirtazapine Treatment
Symptoms associated with the discontinuation or dose reduction of mirtazapine tablets USP have been reported. Patients should be monitored for these and other symptoms when discontinuing treatment or during dosage reduction. A gradual reduction in the dose over several weeks, rather than abrupt cessation, is recommended whenever possible. If intolerable symptoms occur following a decrease in the dose or upon discontinuation of treatment, dose titration should be managed on the basis of the patient’s clinical response (see PRECAUTIONS and ADVERSE REACTIONS).
Information for Patients
Patients should be advised that taking mirtazapine tablets USPcan cause mild pupillary dilation, which in susceptible individuals, can lead to an episode of angle-closure glaucoma. Preexisting glaucoma is almost always open-angle glaucoma because angle-closure glaucoma, when diagnosed, can be treated definitively with iridectomy. Open-angle glaucoma is not a risk factor for angle-closure glaucoma. Patients may wish to be examined to determine whether they are susceptible to angle-closure, and have a prophylactic procedure (e.g., iridectomy), if they are susceptible.

No Recall
Chain Drug Consortium

Hand Wash | Chain Drug Consortium

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Meijer Distribution Inc

Hand Wash | Meijer Distribution Inc

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall
Meijer Distribution

Hand Wash | Meijer Distribution

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

No Recall