TYLENOL PM- acetaminophen and diphenhydramine hydrochloride tablet, film coated 
Select Corporation

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.

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Tylenol® PM

Drug Facts

Active ingredients (in each caplet)Purpose
Acetaminophen 500 mgPain reliever
Diphenhydramine HCl 25 mgNighttime 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

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.

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
  • if you have ever had an allergic reaction to this product or any of its ingredients

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 serious underlying medical illness.
  • pain 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

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

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 yearsdo not use

Other information

Inactive ingredients

carnauba wax, crospovidone, FD&C blue no. 1 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, stearic acid, titanium dioxide

Questions or comments?

call 1-877-895-3665 (toll-free) or 215-273-8755 (collect)

Distributed by:
McNeil Consumer Healthcare
Division of McNEIL-PPC, Inc.
Fort Washington, PA 19034 USA

PRINCIPAL DISPLAY PANEL - 2 Caplet Pouch Carton

Extra Strength

TYLENOL®
PM

Acetaminophen, Diphenhydramine HCl
Pain Reliever, Nighttime Sleep Aid
Non-habit forming

Contains No Aspirin

50 Pouches of
2 Caplets each

PRINCIPAL DISPLAY PANEL - 2 Caplet Pouch Carton
TYLENOL PM 
acetaminophen and diphenhydramine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52904-945(NDC:50580-608)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
acetaminophen (UNII: 362O9ITL9D) (acetaminophen - UNII:362O9ITL9D) acetaminophen500 mg
diphenhydramine hydrochloride (UNII: TC2D6JAD40) (diphenhydramine - UNII:8GTS82S83M) diphenhydramine hydrochloride25 mg
Inactive Ingredients
Ingredient NameStrength
carnauba wax (UNII: R12CBM0EIZ)  
crospovidone (UNII: 2S7830E561)  
FD&C blue no. 1 aluminum lake (UNII: J9EQA3S2JM)  
hypromellose, unspecified (UNII: 3NXW29V3WO)  
magnesium stearate (UNII: 70097M6I30)  
microcrystalline cellulose (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
polysorbate 80 (UNII: 6OZP39ZG8H)  
povidone, unspecified (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
stearic acid (UNII: 4ELV7Z65AP)  
titanium dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorBLUE (Light Blue) Scoreno score
ShapeOVALSize19mm
FlavorImprint Code TY;PM
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52904-945-041 in 1 BLISTER PACK03/01/1997
12 in 1 POUCH; Type 0: Not a Combination Product
2NDC:52904-945-052 in 1 BLISTER PACK03/01/1997
22 in 1 POUCH; Type 0: Not a Combination Product
3NDC:52904-945-2020 in 1 CARTON03/01/1997
32 in 1 POUCH; Type 0: Not a Combination Product
4NDC:52904-945-2525 in 1 CARTON03/01/1997
42 in 1 POUCH; Type 0: Not a Combination Product
5NDC:52904-945-5050 in 1 CARTON03/01/1997
52 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34303/01/1997
Labeler - Select Corporation (053805599)

Revised: 3/2022
Document Id: 786973d9-0cfa-4a49-97ea-10dab5ac0cec
Set id: 5b050993-334c-4118-865c-aae980b48aed
Version: 1
Effective Time: 20220325
 
Select Corporation