DrugCite

PAIN RELIEVER PM EXTRA STRENGTH - acetaminophen and diphenhydramine hydrochloride tablet 
McKesson (Sunmark)

Extra Strength Acetaminophen PM

DRUG FACTS

Active ingredients (in each caplet)

Acetaminophen 500 mg

Diphenhydramine HCl 25 mg

Purpose

Pain reliever

Nighttime sleep- aid

Uses

temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness.

Warnings

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

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

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.
  • with any other product containing diphenhydramine, even one used on skin
  • in children under 12 years of age

Ask a doctor before use if you have

  • liver disease
  • a breathing problem such as emphysema or chronic bronchitis
  • trouble urinating due to an enlarged prostate gland
  • glaucoma

Ask a doctor or pharmacist before use if you are

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

When using this product

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

Stop use and ask a doctor if

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

These could be signs of a serious condition

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

  • do not take more than directed (see overdose warning)
adults and children 12 years and over
  •  take 2 caplets at bedtime. Do not take more than 2 caplets of this product in 24 hours
children under 12 years
  • Do not use

Other information

  • store at room temperature 15°-30°C (59°-86°F)
  • avoid high humidity and excessive heat

Inactive ingredients

croscarmellose sodium*, D and C Yellow #10 Aluminum Lake*, FD and C Blue #1 Aluminum Lake, FD and C Blue #2 Aluminum Lake*, hypromellose, magnesium silicate*, magnesium stearate*, microcrystalline cellulose*, mineral oil*, polyethylene glycol*, povidone, pregelatinized starch, silica*, sodium starch glycolate*, stearic acid, titanium dioxide, triacetin*

*contains one or more of these ingredients

Questions or Comments?

Call 1-877-753-3935 Monday- Friday 9AM- 5PM EST

Principal Display Panel

Compare to EXTRA STRENTH Tylenol® PM active ingredients **

Pain Reliever PM

Extra Strength

Pain reliever /nighttime Sleep-Aid

Non- habit forming

Acetaminophen 500 mg

Diphenhydramine HCl 25 mg

Tamper Evident: Do not use if imprinted safety seal under cap is broken or missing

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

**This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Tylenol® PM.

Mckesson sunmark

Pain Reliever PM caplets



PAIN RELIEVER PM  EXTRA STRENGTH
acetaminophen, diphenhydramine hcl  tablet
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 49348-236
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 500 mg
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM  
FD&C BLUE NO. 1  
FD&C BLUE NO. 2  
HYPROMELLOSES  
MAGNESIUM STEARATE  
CELLULOSE, MICROCRYSTALLINE  
POLYETHYLENE GLYCOLS  
POVIDONES  
STEARIC ACID  
TITANIUM DIOXIDE  
D&C YELLOW NO. 10  
MAGNESIUM SILICATE  
MINERAL OIL  
STARCH, CORN  
SILICON DIOXIDE  
SODIUM STARCH GLYCOLATE TYPE A CORN  
TRIACETIN  
Product Characteristics
Color BLUE Score no score
Shape CAPSULE Size 18mm
Flavor Imprint Code S525;CPC752
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 49348-236-10 1 BOTTLE In 1 BOX contains a BOTTLE
1 100 TABLET In 1 BOTTLE This package is contained within the BOX (49348-236-10)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part343 03/26/2013

Labeler - McKesson (Sunmark) (177667227)
Registrant - P and L Development of New York Corporation (800014821)
Revised: 04/2013McKesson (Sunmark)