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Wal-Nadol PM

Dosage form: tablet, film coated
Ingredients: ACETAMINOPHEN 500mg, DIPHENHYDRAMINE HYDROCHLORIDE 25mg
Labeler: WALGREEN CO.
NDC Code: 0363-0235

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.

Walgreens 44-235

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

  • if you are allergic to acetaminophen or any of the inactive ingredients in this product

  • in children under 12 years of age

Ask a doctor before use if
  • a breathing problem such as emphysema or chronic bronchitis

  • liver disease

  • 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 beverages

  • 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 more than 10 days

  • fever gets worse or lasts 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: Taking more than the recommended dose (overdose) may cause liver damage. 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
  • 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 this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.

Other information
  • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)

  • see end flap for expiration date and lot number

Inactive ingredients

colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C blue #1, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, stearic acid, talc, titanium dioxide

Questions or comments?

1-800-426-9391

Product Packaging

Well at
Walgreens
WALGREENS PHARMACIST RECOMMENDEDǂ

NDC 0363-235-08

Wal-Nadol PM
Acetaminophen
500 mg / Pain Reliever
DIphenhydramine HCl 25 mg / Nighttime Sleep Aid

24 CAPLETS 

Compare to Panadol® PM Extra Strength Caplets active ingredientsǂǂ

ǂWalgreens Pharmacist Survey Study, November 2010
ǂǂThis product is not manufactured  or distributed by GlaxoSmithKline Consumer Health, owner of the registered trademark Panadol® PM Extra Strength Caplets.
50844    REV0512A23508

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Walgreens 44-235 Wal-Nadol PM

WAL-NADOL PM 
acetaminophen and diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0235
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN500 mg
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE 
CROSCARMELLOSE SODIUM 
FD&C BLUE NO. 1 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOLS 
POLYVINYL ALCOHOL 
POVIDONES 
STEARIC ACID 
TALC 
TITANIUM DIOXIDE 
Product Characteristics
ColorBLUEScoreno score
ShapeCAPSULESize17mm
FlavorImprint Code44;235
Contains    
Packaging
#Item CodePackage Description
1NDC:0363-0235-571 BOTTLE, PLASTIC (1 BOTTLE) in 1 CARTON
1125 TABLET, FILM COATED (125 TABLET) in 1 BOTTLE, PLASTIC
2NDC:0363-0235-151 BOTTLE, PLASTIC (1 BOTTLE) in 1 CARTON
250 TABLET, FILM COATED (50 TABLET) in 1 BOTTLE, PLASTIC
3NDC:0363-0235-291 BOTTLE, PLASTIC (1 BOTTLE) in 1 CARTON
3150 TABLET, FILM COATED (150 TABLET) in 1 BOTTLE, PLASTIC
4NDC:0363-0235-081 BOTTLE, PLASTIC (1 BOTTLE) in 1 CARTON
424 TABLET, FILM COATED (24 TABLET) in 1 BOTTLE, PLASTIC
5NDC:0363-0235-121 BOTTLE, PLASTIC (1 BOTTLE) in 1 CARTON
5100 TABLET, FILM COATED (100 TABLET) in 1 BOTTLE, PLASTIC
6NDC:0363-0235-13250 TABLET, FILM COATED (250 TABLET) in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34305/15/1994
Labeler - WALGREEN CO. (008965063)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.832867894MANUFACTURE(0363-0235)
Establishment
NameAddressID/FEIOperations
LNK International, Inc.038154464PACK(0363-0235)

Revised: 10/2013
 
WALGREEN CO.

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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