VICKS PAINQUIL PM LIQUICAPS PAIN RELIEVER PLUS NIGHTTIME SLEEP-AID- acetaminophen, diphenhydramine hcl capsule, liquid filled

Vicks PainQuil PM by

Drug Labeling and Warnings

Vicks PainQuil PM by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredients (in each LiquiCap)

Acetaminophen 500 mg
Diphenhydramine HCl 25 mg

Purpose

Pain reliever

Nighttime sleep-aid

Use

• for the temporary relief of occasional minor aches and pains with accompanying sleeplessness.

Warnings

Liver warning:

This product contains acetaminophen. Severe liver damage may occur if you take

• more than 3 doses (2 LiquiCaps each) in 24 hours, which is the maximum daily amount for this product
• with other drugs containing acetaminophen
• 3 or more alcoholic drinks every day while using this product

Allergy Alert:

Acetaminophen may cause severe skin reactions. Symptoms may include:

• skin reddening
• blisters
• rash

If a skin reaction occurs, stop use and seek medical help right away

Sore throat warning:

If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use

• with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
• for children under 12 years of age
• with any other product containing diphenhydramine, even one used on skin

Ask a doctor before use if you have

• liver disease
• a breathing problem such as emphysema or chronic bronchitis
• glaucoma
• difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

• taking the blood thinning drug warfarin
• taking sedatives or tranquilizers

Stop use and ask a doctor if

• pain or cough gets worse or lasts more than 10 days
• fever gets worse or lasts more than 3 days
• redness or swelling is present
• new symptoms occur
• Sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness.

These could be signs of a serious condition.

When using this product

• avoid alcoholic beverages
• drowsiness will occur
• do not drive a motor vehicle or operate machinery

If pregnant or breast-feeding,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OVERDOSAGE

In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

• take only one dose (2 LiquiCaps) per day (24 hours)

• adults & children 12 yrs & over: 2 LiquiCaps at bedtime
• children under 12 yrs: do not use

Other information

store at no greater than 25°C (77°F)

Inactive ingredients

1,4 sorbitan, D&C Red No. 33, FD&C Blue No. 1, gelatin, glycerin, mannitol, polyethylene glycol 400, polyethylene glycol 600, polyvinyl acetate phthalate, povidone, propylene glycol, sorbitol, titanium dioxide, water

Questions?

1-877-881-5813

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TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS MISSING OR DAMAGED.

‡Maximum strength dose of active ingredients per dosing interval, only use as directed.

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DIST. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 100 LiquiCaps™

MAX STRENGTH‡

VICKS®

PainQuil™ PM

LIQUICAPS™

PAIN RELIEVER 

+ NIGHTTIME SLEEP-AID

Acetaminophen, Diphenhydramine HCl

STARTS WORKING FAST

FOR RELIEF OF:

ACHES | PAINS | HEADACHE | SORE THROAT | 

+ OCCASSIONAL SLEEPLESSNESS

100 LIQUICAPS™

INGREDIENTS AND APPEARANCE

VICKS PAINQUIL PM  LIQUICAPS PAIN RELIEVER PLUS NIGHTTIME SLEEP-AID
acetaminophen, diphenhydramine hcl capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84126-375
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg
DIPHENHYDRAMINE HCL (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HCL	25 mg

Inactive Ingredients
Ingredient Name	Strength
POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GELATIN (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POVIDONE (UNII: FZ989GH94E)
1,4-SORBITAN (UNII: AV0YTZ4E6J)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
MANNITOL (UNII: 3OWL53L36A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	purple	Score	no score
Shape	OVAL	Size	19mm
Flavor		Imprint Code	PQPM
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84126-375-01	1 in 1 CARTON	03/17/2026
1		100 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	03/17/2026

Labeler - The Procter & Gamble Manufacturing Company (004238200)