Drugplain

daytime 325 mg/1

Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl · CAPSULE, LIQUID FILLED · Publix Super Markets Inc

10 Recalls on RecordCurrently in Shortage
Plain English

daytime is a capsule, liquid filled containing acetaminophen, dextromethorphan hbr, phenylephrine hcl at 325 mg/1, taken oral. Manufactured by Publix Super Markets Inc.

Key Facts

Brand Name
daytime
Generic Name
Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl
NDC Code (Product)
56062-417
Manufacturer
Publix Super Markets Inc
Strength
325 mg/1
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
08/30/2018

Recall History

10 Recalls on Record
Class II06/18/2013

Novartis Consumer Health

Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

TerminatedVoluntary: Firm initiated
Class III03/09/2018

Alva-Amco Pharmacal Companies., Inc.

Subpotent Drug: The product has failed to maintain its label claim of coal tar throughout its labeled 24-month expiry period.

TerminatedVoluntary: Firm initiated
Class II06/18/2013

Novartis Consumer Health

Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

TerminatedVoluntary: Firm initiated
Class III02/18/2013

L. Perrigo Co.

Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.

TerminatedVoluntary: Firm initiated
Class III09/02/2021

New Vision Pharmaceuticals LLC

Subpotent Drug

TerminatedVoluntary: Firm initiated
Class III05/15/2013

Novartis Consumer Health

Failed Impurities/Degradation:Specifications:Unknown degradant found during stability testing.

TerminatedVoluntary: Firm initiated
Class III09/02/2021

New Vision Pharmaceuticals LLC

Subpotent Drug

TerminatedVoluntary: Firm initiated
Class III06/05/2017

L. Perrigo Company

Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Cough Liquid.

TerminatedVoluntary: Firm initiated
Class II06/18/2013

Novartis Consumer Health

Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.

TerminatedVoluntary: Firm initiated
Class III04/25/2014

Prestige Brands Holdings

Presence of Precipitate; small amounts of diphenhydramine precipitated out of solution

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug abuse754 reports
toxicity to various agents696 reports
completed suicide374 reports
death326 reports
drug interaction216 reports
dyspnoea198 reports
overdose187 reports
pneumonia181 reports
drug ineffective178 reports
off label use166 reports

Frequently Asked Questions

What is daytime used for?

daytime contains Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is daytime a controlled substance?

daytime is not classified as a controlled substance by the DEA.

What is the generic name for daytime?

The generic name for daytime is Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl. There are 12 other brand versions of Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl.

What is the NDC code for daytime 325 mg/1?

The NDC (National Drug Code) for daytime 325 mg/1 is 56062-417, listed by Publix Super Markets Inc.