FLU HBP MAXIMUM STRENGTH (acetaminophen, chlorpheniramine maleate, dextromethorphan hbr) tablet, film coated [Meijer Distribution Inc]

meijer®

NDC 41250-638-09
Compare to Coricidin® HBPMaximum Strength Fluactive ingredients*

MAXIMUM STRENGTH

flu HBP

Acetaminophen 325 mg
Chlorpheniramine maleate 2 mgDextromethorphan HBr 10 mgPain Reliever/Fever ReducerAntihistamineCough Suppressant
For People with High Blood Pressure
Relieves: Body Aches, Pains & Headache,Fever, Cough, Runny Nose, Sore Throat, Sneezing

20 Caplets
ActualSize

TAMPER EVIDENT: DO NOT USE IF PACKAGEIS OPENED OR IF BLISTER UNIT IS TORN, BROKENOR SHOWS ANY SIGNS OF TAMPERING

DIST. BY MEIJERDISTRIBUTION, INC.GRAND RAPIDS, MI 49544www.meijer.com

*This product is not manufactured ordistributed by Bayer HealthCare LLC,owner of the registered trademarkCoricidin® HBP Maximum Strength Flu.50844           ORG101973809

Meijer 44-738

METOPROLOL SUCCINATE tablet, film coated, extended release [Cardinal Health]

In five controlled studies in normal healthy subjects, the same daily doses of metoprolol succinate extended-release tablets and immediate-release metoprolol were compared in terms of the extent and duration of beta 1-blockade produced. Both formulations were given in a dose range equivalent to 100 mg to 400 mg of immediate-release metoprolol per day. In these studies, metoprolol succinate extended-release tablets were administered once a day and immediate-release metoprolol was administered once to four times a day. A sixth controlled study compared the beta 1-blocking effects of a 50 mg daily dose of the two formulations. In each study, beta 1-blockade was expressed as the percent change from baseline in exercise heart rate following standardized submaximal exercise tolerance tests at steady…

ARISTADA (aripiprazole lauroxil) injection, suspension, extended release [Alkermes, Inc.]

5.1 Increased Mortality in Elderly Patients with Dementia-related Psychosis

Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of 17 placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in the placebo group.

Although the causes of death were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. Observational studies…

DEFENSOLITO CHILDREN SYRUP (guaifenesin, dextromethorphan hbr) liquid [Menper Distributors, Inc.]

To receive this label RSS feed Copy the URL below and paste it into your RSS Reader application. https://dailymed.nlm.nih.gov/dailymed/labelrss.cfm?setid=1077131e-c8b9-4f68-aa1e-191075cc97ca To receive all DailyMed Updates for the last seven days Copy the URL below and paste it into your RSS Reader application. https://dailymed.nlm.nih.gov/dailymed/rss.cfm What will I get with the DailyMed RSS feed? DailyMed will deliver notification of updates and additions to Drug Label information currently shown on this site through its RSS feed. DailyMed will deliver this notification to your desktop, Web browser, or e-mail depending on the RSS Reader you select to use. To view updated drug label links, paste the RSS feed address (URL) shown below into a RSS reader, or use a browser which supports RSS feeds, such…

CARDENE IV (nicardipine hydrochloride) injection, solution [Chiesi USA, Inc.]

Cardene (nicardipine hydrochloride) is a calcium ion influx inhibitor (slow channel blocker or calcium channel blocker).  Cardene I.V. Premixed Injection for intravenous administration contains 20 mg (0.1 mg/mL) of nicardipine hydrochloride per 200 mL in either dextrose or sodium chloride or 40 mg (0.2 mg/mL) of nicardipine hydrochloride per 200 mL in sodium chloride.  Nicardipine hydrochloride is a dihydropyridine derivative with IUPAC (International Union of Pure and Applied Chemistry) chemical name (±)-2-(benzyl-methyl amino) ethyl methyl 1,4-dihydro-2,6-dimethyl-4-(m-nitrophenyl)-3,5-pyridinedicarboxylate monohydrochloride and has the following structure:

Nicardipine hydrochloride is a greenish-yellow, odorless, crystalline powder that melts at about 169ºC.  It is freely soluble in chloroform, methanol, and glacial acetic acid, sparingly soluble in anhydrous ethanol, slightly soluble in n-butanol, water, 0.01 M potassium dihydrogen phosphate, acetone,…

LA FLECHA JAPONESA (methyl salicylate) oil [Menper Distributors, Inc.]

To receive this label RSS feed Copy the URL below and paste it into your RSS Reader application. https://dailymed.nlm.nih.gov/dailymed/labelrss.cfm?setid=08819ad0-97c2-49bd-b923-535b94a27167 To receive all DailyMed Updates for the last seven days Copy the URL below and paste it into your RSS Reader application. https://dailymed.nlm.nih.gov/dailymed/rss.cfm What will I get with the DailyMed RSS feed? DailyMed will deliver notification of updates and additions to Drug Label information currently shown on this site through its RSS feed. DailyMed will deliver this notification to your desktop, Web browser, or e-mail depending on the RSS Reader you select to use. To view updated drug label links, paste the RSS feed address (URL) shown below into a RSS reader, or use a browser which supports RSS feeds, such…

CEFAZOLIN injection, powder, for solution [WG Critical Care, LLC]

Usual Adult Dosage:
* In rare instances, doses of up to 12 grams of Cefazolin for Injection per day have been used.

Perioperative Prophylactic Use: To prevent postoperative infection in contaminated or potentially contaminated surgery, recommended doses are:

a.
1 gram I.V. or I.M. administered ½ hour to 1 hour prior to the start of surgery.
b.
For lengthy operative procedures (e.g., 2 hours or more), 500 mg to 1 gram I.V. or I.M. during surgery (administration modified depending on the duration of the operative procedure).
c.
500 mg to 1 gram I.V. or I.M. every 6 to 8 hours for 24 hours postoperatively.

It is important that (1) the preoperative dose be given just prior (1/2 hour to 1 hour) to the start of surgery so that…

PAROXETINE (paroxetine hydrochloride hemihydrate) tablet, film coated [REMEDYREPACK INC.]

Associated With Discontinuation of Treatment: Twenty percent (1,199/6,145) of patients treated with Paroxetine Tablets in worldwide clinical trials in major depressive disorder and 16.1% (84/522), 11.8% (64/542), 9.4% (44/469) and 10.7% (79/735) of patients treated with Paroxetine Tablets in worldwide trials in social anxiety disorder, OCD, panic disorder and GAD, respectively, discontinued treatment due to an adverse event. The most common events (≥1%) associated with discontinuation and considered to be drug related (i.e., those events associated with dropout at a rate approximately twice or greater for Paroxetine Tablets compared to placebo) included the following:

Commonly Observed Adverse Events: Major Depressive Disorder: The most commonly observed adverse events associated with the use of paroxetine (incidence of 5%…

NICOTINE (nicotine polacrilex) lozenge [Rite Aid Corporation]

Compare to the active ingredient in Nicorette® Lozenge*

Nicotine Lozenges

Nicotine Polacrilex Lozenge
Stop Smoking Aid
Mint Flavor

FOR THOSE WHO SMOKE THEIR FIRST CIGARETTE WITHIN 30 MINUTES OF WAKING UP.

If you smoke your first cigarette MORE THAN 30 MINUTES after waking up, use Nicotine Polacrilex 2 mg Lozenge.

LOZENGES, 4 mg Each

TO INCREASE YOUR SUCCESS IN QUITTING:

1. You must be motivated to quit.

2. Use Enough – Use at least 9 Nicotine Polacrilex lozenges per day during the first six weeks.

3. Use Long Enough – Use Nicotine Polacrilex lozenges for the full 12 weeks.

4. Use With a Support Program as directed in the enclosed User’s Guide.

not for sale to those under 18 years of age

proof of age required

not for sale in vending machines or from any source where proof…

CLEOCIN PHOSPHATE (clindamycin phosphate) injection, solution CLEOCIN PHOSPHATE (0009-6582) (STANDALONE) (clindamycin phosphate) injection, solution [Pharmacia and Upjohn Company LLC]

CLEOCIN PHOSPHATE products are indicated in the treatment of serious infections caused by susceptible anaerobic bacteria.
CLEOCIN PHOSPHATE products are also indicated in the treatment of serious infections due to susceptible strains of streptococci, pneumococci, and staphylococci. Its use should be reserved for penicillin-allergic patients or other patients for whom, in the judgment of the physician, a penicillin is inappropriate. Because of the risk of antibiotic-associated pseudomembranous colitis, as described in the BOXED WARNING, before selecting clindamycin the physician should consider the nature of the infection and the suitability of less toxic alternatives (e.g., erythromycin).
Bacteriologic studies should be performed to determine the causative organisms and their susceptibility to clindamycin.
Indicated surgical procedures should be performed in conjunction with antibiotic therapy.
CLEOCIN PHOSPHATE is…