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Pain Relief PM (Target Corporation)

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TABLET 1 BOTTLE, PLASTIC in 1 CARTON (11673-373-12) > 100 TABLET in 1 BOTTLE, PLASTIC Label Information

Complete Pain Relief PM Information

  • Active ingredients

    Acetaminophen 500 mg

    Diphenhydramine citrate 38 mg


  • Purpose

    Pain reliever

    Nighttime sleep-aid


  • Uses

    for the 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 containin diphenhydramine, even one used on skin

    • 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
    • taking sedatives or tranquilizers

    • taking the blood thinning drug warfarin

    When using this product
    • drowsiness may occur

    • avoid alcoholic beverages

    • be careful when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if
    • sleeplessness lasts continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness.

    • pain gets worse or lasts more than 10 days

    • fever gets worse or lasts more than 3 days

    • new symptoms occur

    • painful area is red or swollen

    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 tablets at bedtime. Do not take more than 2 tablets 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 controlled room temperature 15°-30°C (59°-86°F)

    • see end flap for expiration date and lot number


  • Inactive ingredients

    corn starch, croscarmellose sodium, crospovidone, FD&C blue #1 aluminum lake, FD&C blue #2 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, shellac, silica gel, stearic acid, titanium dioxide


  • Questions

    1-800-426-9391


  • Principal Display Panel

    NDC 11673-373-12

    pain relief pm

    acetaminophen, 500 mg

    diphenhydramine citrate, 38 mg

    Compare to active ingredients in Excedrin® PM*

    pain reliever/

    nighttime sleep aid

    aspirin free

    up & upâ„¢

    100 COATED TABLETS

    ACTUAL SIZE

    *This product is not manufactured or distributed by Novartis Consumer Health, Inc., owner of the registered trademark Excedrin® PM.

    50844    ORG031037312

    094    01    0739    ID282426

    Distributed by Target Corporation

    Minneapolis, MN 55403

    ©2012 Target Brands, Inc.

    Shop Target.com

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

    Target 44-373

    Target 44-373


  • INGREDIENTS AND APPEARANCE
    PAIN RELIEF PM 
    acetaminophen and diphenhydramine citrate tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-373
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
    DIPHENHYDRAMINE CITRATE (UNII: 4OD433S209) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE CITRATE 38 mg
    Inactive Ingredients
    Ingredient Name Strength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color BLUE Score no score
    Shape ROUND Size 11mm
    Flavor Imprint Code 44;373
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-373-12 1 in 1 CARTON
    1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part343 06/07/2004 11/04/2018
    Labeler - Target Corporation (006961700)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(11673-373)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(11673-373)