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Allergy Relief Multisymptom

Dosage form: tablet, coated
Ingredients: ACETAMINOPHEN 325mg, CHLORPHENIRAMINE MALEATE 2mg, PHENYLEPHRINE HYDROCHLORIDE 5mg
Labeler: Select Corporation
NDC Code: 52904-457

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active Ingredients

Acetaminophen 325 mg.......................Pain Reliever/Fever Reducer
Chlorpheniramine Maleate 2 mg.............................Antihistamine
Phenylephrine HCl 5 mg.............................Nasal Decongestant



Pain Reliever, Fever Reducer, Antihistamine, Nasal Decongestant

Directions: Adults and children 12 years of age and older • take 2
tablets every 4 to 6 hours as needed, do not exceed 8 tablets in 24 hours, or
as directed by a doctor • Children under 12 years, consult a doctor

Uses: Temporarily: • relieves nasal congestion associated with sinusitis
• relieves nasal congestion due to the common cold, hay fever or other
upper respiratory allergies • relieves sinus congestion and pressure,
helps decongest sinus openings and passages • restores free breathing
• helps loosen phlegm (mucus) and thin bronchial secretions to rid the
bronchial passages of bothersome mucus, drain bronchial tubes, and
make coughs more productive • Temporarily relieves minor aches, pains,
and fever associated with: • headache • common cold • toothache
• backache • muscular aches • menstrual cramps

Warnings: Liver Warning: This
product contains acetaminophen. Severe liver damage may occur if
you take: • more than 8 tablets in 24 hours • with other drugs containing
acetaminophen (prescription or nonprescription). Ask a doctor or
pharmacist before using with other drugs if you are not sure. • 3 or more
alcoholic drinks every day while using this product Do not: use with
any other product containing acetaminophen this will provide more
than the recommended dose (overdose) of acetaminophen and could
cause serious health concerns. • use more than the recommended
dose • for more than 10 days for pain unless directed by a doctor • for
more than 3 days for fever unless directed by a doctor • if you are now
taking a prescription monoamine oxidase inhibitor (MAOI)
(certain drugs for depression, psychiatric or emotional
conditions, or Parkinson’s disease), or for 2 weeks after
stopping MAOI drug. If you do not know if your prescription
drug contains an MAOI, consult a doctor or pharmacist before
taking this product. Stop use and ask a doctor if: • symptoms
do not improve • pain or fever persists or gets worse • new
symptoms occur • redness or swelling is present • nervousness,
dizziness or sleeplessness occur • symptoms do not improve within 7
days or are accompanied by fever Ask a doctor before use if you
have: • heart disease • high blood pressure • thyroid disease • diabetes
• difficulty in urination due to enlargement of the prostate gland • a breathing
problem such as emphysema or chronic bronchitis, or if you have glaucoma
or difficulty in urination due to enlargement of the prostate gland • may cause
excitability especially in children • may cause drowsiness; alcohol, sedatives,
and tranquilizers may increase the drowsiness effect • avoid alcoholic
beverages while taking this product • do not take this product if you are
taking sedatives or tranquilizers, without first consulting your doctor • use
caution when operating machinery.

If pregnant or breast-feeding baby, ask a health professional
before use.

KEEP OUT OF REACH OF CHILDREN.

Inactive ingredients: FDC Red 40,
Maltodextrin, Microcrystalline Cellulose, Povidone, Sodium Starch
Glycolate, Starch, Stearic Acid

MM1

ALLERGY RELIEF MULTISYMPTOM  
acetaminophen,chlorpheniramine maleate, phenylephrine hcl tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52904-457
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN325 mg
CHLORPHENIRAMINE MALEATE (CHLORPHENIRAMINE) CHLORPHENIRAMINE MALEATE2 mg
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE5 mg
Inactive Ingredients
Ingredient NameStrength
POVIDONE K29/32 
SODIUM STARCH GLYCOLATE TYPE A POTATO 
CELLULOSE, MICROCRYSTALLINE 
STEARIC ACID 
MALTODEXTRIN 
STARCH, CORN 
Product Characteristics
Colorwhite (snow white) Scoreno score
ShapeROUND (FR11) Size11mm
FlavorImprint CodeFR11
Contains    
Packaging
#Item CodePackage Description
1NDC:52904-457-022 TABLET, COATED (TABLET) in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/15/2012
Labeler - Select Corporation (053805599)

Revised: 10/2012
 
Select Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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