Drugplain

GUAIFENESIN 100 mg/5mL

GUAIFENESIN · SOLUTION · PAI Holdings, LLC dba PAI Pharma

10 Recalls on Record
Plain English

GUAIFENESIN is a solution containing guaifenesin at 100 mg/5mL, taken oral. Manufactured by PAI Holdings, LLC dba PAI Pharma.

Key Facts

Brand Name
GUAIFENESIN
Generic Name
GUAIFENESIN
NDC Code (Product)
0121-0744
Manufacturer
PAI Holdings, LLC dba PAI Pharma
Strength
100 mg/5mL
Dosage Form
SOLUTION
Route
ORAL
Marketing Status
Application #
M012
Drug Class
Expectorant [EPC]
Marketing Start
09/01/2002

Recall History

10 Recalls on Record
Class III04/11/2014

Aaron Industries Inc

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.

TerminatedVoluntary: Firm initiated
Class III01/18/2013

Aaron Industries Inc

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.

TerminatedVoluntary: Firm initiated
Class II02/16/2024

Global Corporation

Stability testing failures for one or two of the four active pharmaceutical ingredients among the finished drug products, i.e., Phenylephrine HCL, and/or Chlorpheniramine Maleate.

OngoingVoluntary: Firm initiated
Class II07/02/2013

Aidapak Services, LLC

Labeling:Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as MISOPROSTOL, Tablet, 200 mcg, NDC 59762500801, Pedigree: AD21965_13, EXP: 5/1/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: AD56917_7, EXP: 5/21/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD73627_17, EXP: 5/30/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: W003216

TerminatedVoluntary: Firm initiated
Class I04/15/2015

Reckitt Benckiser LLC

Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result certain safety warnings associated with those ingredients may also be missing.

TerminatedVoluntary: Firm initiated
Class II01/08/2016

Perrigo Company PLC

Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.

TerminatedVoluntary: Firm initiated
Class III01/07/2025

PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Superpotent; sodium benzoate preservative

CompletedVoluntary: Firm initiated
Class II11/07/2024

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Failed Impurity/Degradation Specifications

TerminatedVoluntary: Firm initiated
Class II01/24/2022

Ultra Seal Corporation

cGMP deviations

TerminatedVoluntary: Firm initiated
Class II05/21/2019

Torrent Pharma Inc

cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

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

dyspnoea648 reports
drug ineffective624 reports
pneumonia602 reports
nausea574 reports
fatigue542 reports
diarrhoea540 reports
pain489 reports
headache442 reports
cough440 reports
off label use422 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses ■ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Dosage & Administration

Directions ■ do not crush, chew, or break tablet ■ take with a full glass of water ■ this product can be administered without regard for timing of meals ■ adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours. ■ children under 12 years of age: do not use

Warnings

Warnings Do not use ■ for children under 12 years of age

Frequently Asked Questions

What is GUAIFENESIN used for?

GUAIFENESIN contains GUAIFENESIN. It is a solution taken oral. Consult your doctor for specific uses.

Is GUAIFENESIN a controlled substance?

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

What is the generic name for GUAIFENESIN?

The generic name for GUAIFENESIN is GUAIFENESIN. There are 12 other brand versions of GUAIFENESIN.

What is the NDC code for GUAIFENESIN 100 mg/5mL?

The NDC (National Drug Code) for GUAIFENESIN 100 mg/5mL is 0121-0744, listed by PAI Holdings, LLC dba PAI Pharma.