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Pill Identifier Information of ASA 81 MG Delayed Release Tablet

Drug Information

ASA 81 MG Delayed Release Tablet

Imprint: L277
Shape: C48348
Color: C48331
Ingredients: Aspirin
Size: 7.00
Score: 1
Rxtty: SY
Author: Time-Cap Labs, Inc
Inactive Ingredients: ANHYDROUS LACTOSE / FERROSOFERRIC OXIDE / CARNAUBA WAX / SILICON DIOXIDE / CROSCARMELLOSE SODIUM / FD&C RED NO. 40 / FD&C YELLOW NO. 6 / FERRIC OXIDE YELLOW / METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A / CELLULOSE, MICROCRYSTALLINE / POLYSORBATE 80 / POTASSIUM HYDROXIDE / PROPYLENE GLYCOL / SHELLAC / DIMETHICONE / SODIUM HYDROXIDE / SODIUM LAURYL SULFATE / TALC / TRIETHYL CITRATE>

Complete Information

  • ACTIVE INGREDIENT

    Active ingredient (in each tablet)


    Aspirin 81 mg (NSAID*)

    *nonsteroidal anti-inflammatory drug

  • PURPOSE

    Purpose


    PAIN RELIEVER

  • INDICATIONS & USAGE

    Uses


    • temporarily relieves minor aches and pains
    • for other uses, see your doctor, but do not use for more than 10 days without consulting your doctor because serious side effects may occur
  • WARNINGS

    • Warnings

      Reye's syndrome:

      Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

      Allergy alert:

      Aspirin may cause a severe allergic reaction, which may include:

      hives
      facial swelling
      shock
      asthma (wheezing)
      Stomach bleeding warning:

      This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:

      are age 60 or older
      have had stomach ulcers or bleeding problems
      take a blood thinning (anticoagulant) drug
      take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
      have 3 or more alcoholic drinks every day while using this product
      take more or for a longer time than directed

  • DO NOT USE

    Do not use


    • if you are allergic to aspirin or any other pain reliever/fever reducer
  • ASK DOCTOR

    Ask a doctor before use if

    • stomach bleeding warning applies to you
    • you have a history of stomach problems, such as heartburn
    • you have high blood pressure, heart disease, liver cirrhosis, or kidney disease
    • you are taking a diuretic
    • you have asthma
    • you have not been drinking fluids
  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are

    • taking a prescription drug for diabetes, gout, or arthritis
    • taking any other drug
    • under a doctor's care for any serious condition
  • STOP USE

    Stop use and ask a doctor if

    • you experience any of the following signs of stomach bleeding
      • feel faint
      • have bloody or black stools
      • vomit blood
      • have stomach pain that does not get better
    • pain gets worse or lasts more than 10 days
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present in the painful area
    • any new symptoms appear
    • ringing in the ears or a loss of hearing occurs
  • PREGNANCY OR BREAST FEEDING

    IF pregnant or breast-feeding,

    ask a health professional before use. It is especially important not to use aspirin during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • drink a full glass of water with each dose
    • adults and children 12 years and over: take 4 to 8 tablets every 4 hours not to exceed 48 tablets in 24 hours unless directed by a doctor
    • children under 12 years: consult a doctor
  • STORAGE AND HANDLING

    Other information

    • store at 25°C (77°F) excursions permitted between 15°-30°C (59°-86°F)
    • use by expiration date on package
  • INACTIVE INGREDIENT

    Inactive ingredients

    anhydrous lactose, black iron oxide, carnauba wax, colloidal silicon dioxide, croscarmellose sodium, FD-C red 40 aluminum lake, FD-C yellow 6 aluminum lake, iron oxide ochre, methacrylic acid copolymer, microcrystalline cellulose, polysorbate 80, potassium hydroxide, propylene glycol, shellac, simethicone, sodium hydroxide, sodium lauryl sulfate, triethyl citrate

  • PRINCIPAL DISPLAY PANEL

    ASPIRIN 81MG PEACH TABLETS 349R BULK LABEL

  • INGREDIENTS AND APPEARANCE
    ASPIRIN  DELAYED RELEASE
    aspirin tablet, delayed release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49483-349
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN81 mg  in 81 
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TALC (UNII: 7SEV7J4R1U)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Product Characteristics
    Colororange (PEACH) Scoreno score
    ShapeROUNDSize7mm
    FlavorImprint Code L277
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49483-349-00100000 in 1 CARTON; Type 0: Not a Combination Product12/14/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34312/23/2010
    Labeler - Time-Cap Labs, Inc (037052099)
    Establishment
    NameAddressID/FEIBusiness Operations
    Time-Cap Labs, Inc037052099manufacture(49483-349)
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