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Rapid Release Pain Reliever (Safeway)

Available Formats

Dosage Form Package Information Links
CAPSULE, LIQUID FILLED 1 BOTTLE, PLASTIC in 1 CARTON (21130-519-31) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC Label Information
CAPSULE, LIQUID FILLED 1 BOTTLE, PLASTIC in 1 CARTON (21130-519-12) > 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC Label Information
CAPSULE, LIQUID FILLED 1 BOTTLE, PLASTIC in 1 CARTON (21130-519-29) > 150 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC Label Information
CAPSULE, LIQUID FILLED 1 BOTTLE, PLASTIC in 1 CARTON (21130-519-15) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC Label Information

Complete Rapid Release Pain Reliever Information

  • Active ingredient  (in each gelcap)

    Acetaminophen 500 mg


  • Purpose

    Pain reliever/fever reducer


  • Uses

    • temporarily relieves minor aches and pains due to:
      • headache
      • the common cold
      • backache
      • minor pain of arthritis
      • toothache
      • muscular aches
      • premenstrual and menstrual cramps
    • temporarily reduces fever

  • Warnings

    Liver warning:  This product contains acetaminophen. The maximum daily dose of this product is 6 gelcaps (3,000 mg) in 24 hours. 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.

    Ask a doctor before use if you have

    liver disease.

    Ask a doctor or pharmacist before use if you are

    taking the blood thinning drug warfarin.

    Stop use and ask a doctor if
    • pain gets worse or lasts more than 10 days
    • fever gets worse or lasts more than 3 days
    • new symptoms occur
    • redness or swelling is present

    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 (1-800-222-1222) 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 gelcaps every 6 hours while symptoms last
      • do not take more than 6 gelcaps in 24 hours, unless directed by a doctor
      • do not take for more than 10 days unless directed by a doctor
    • children under 12 years: do not use this adult extra strength product in children under 12 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage

  • Other information

    • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
    • avoid high humidity
    • see end flap for expiration date and lot number

  • Inactive ingredients

    croscarmellose sodium, D&C red #33, FD&C blue #1, FD&C red #40, gelatin, hydroxypropyl cellulose, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, stearic acid, titanium dioxide


  • Questions or comments?

    1-800-426-9391


  • Primary Display Panel

    Extra Strength
    Aspirin Free Pain Relief

    NDC 21130-519-15
    Compare to Extra Strength Tylenol® Rapid Release Gels
    active ingredient*

    Acetaminophen, 500 mg

    • Pain Reliever
    • Fever Reducer
    • Rapid Release Gelcap

    50 GELCAPS

    SAFEWAY®

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

    *This product is not manufactured or distributed by McNeil Consumer Healthcare, distributors of Extra Strength Tylenol® Rapid Release Gels.
    50844   REV0513E51915

    DISTRIBUTED BY SAFEWAY INC.
    P.O. BOX 99, PLEASANTON, CA 94566-0009
    QUALITY & SATISFACTION GUARANTEED
    OR YOUR MONEY BACK
    1-888-SAFEWAY / www.safeway.com

    Safeway 44-519

    Safeway 44-519


  • INGREDIENTS AND APPEARANCE
    EXTRA STRENGTH ASPIRIN FREE PAIN RELIEF 
    acetaminophen tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-519
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
    Inactive Ingredients
    Ingredient Name Strength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GELATIN (UNII: 2G86QN327L)  
    HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONES (UNII: FZ989GH94E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color RED (red, gray and blue) Score no score
    Shape CAPSULE Size 19mm
    Flavor Imprint Code L;5
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:21130-519-12 1 in 1 CARTON
    1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2 NDC:21130-519-15 1 in 1 CARTON
    2 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3 NDC:21130-519-29 1 in 1 CARTON
    3 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4 NDC:21130-519-31 1 in 1 CARTON
    4 80 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 05/10/2004 06/11/2018
    Labeler - Better Living Brands, LLC (009137209)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(21130-519)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(21130-519)