Home > Pill Identifier > ASA 81 MG Delayed Release Tablet

Pill Identifier Information of ASA 81 MG Delayed Release Tablet

Drug Information

ASA 81 MG Delayed Release Tablet

Imprint: heart
Shape: C48348
Color: C48331
Ingredients: Aspirin
Size: 7.00
Score: 1
Rxtty: SY
Author: AAA Pharmaceutical, Inc.
Inactive Ingredients: DIACETYLATED MONOGLYCERIDES / ANHYDROUS LACTOSE / CARNAUBA WAX / SILICON DIOXIDE / CROSCARMELLOSE SODIUM / FD&C RED NO. 40 / FD&C YELLOW NO. 6 / HYPROMELLOSES / HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) / FERRIC OXIDE YELLOW / METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) / CELLULOSE, MICROCRYSTALLINE / MINERAL OIL / POLYETHYLENE GLYCOLS / POLYSORBATE 80 / DIMETHICONE / SODIUM HYDROXIDE / SODIUM LAURYL SULFATE / TALC / TITANIUM DIOXIDE / TRIETHYL CITRATE>

Complete Information

  • 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
    • asthma (wheezing)
    • shock

    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) or steroid 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 if you are allergic to aspirin or any other pain reliever/fever reducer

    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

    Ask a doctor or pharmacist before use if you are taking a prescription drug for:

    • diabetes
    • gout
    • arthritis

    Stop use and ask a doctor if
  • pain gets worse or lasts for more than 10 days
  • redness or swelling is present
  • new symptoms occur
  • ringing in the ears or loss of hearing occurs

    • These could be signs of a serious condition.

    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. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • Directions

  • Other information

  • Inactive ingredients

    anhydrous lactose, 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, simethicone, sodium hydroxide, sodium lauryl sulfate, talc, triethyl citrate

  • PRINCIPAL DISPLAY PANEL

    RESTORE u

    NDC 57344-146-08

    †COMPARE TO THE ACTIVE
    INGREDIENT IN ST JOSEPH® LOW DOSE ASPIRIN

    ADULT LOW DOSE

    Safety Coated

    Aspirin
    Pain Reliever
    (NSAID)

    81mg each

    120 ENTERIC COATED TABLETS

    image description

  • INGREDIENTS AND APPEARANCE
    ASPIRIN 
    aspirin tablet, delayed release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57344-146
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN81 mg
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    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 heart
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57344-146-081 in 1 CARTON09/01/2017
    1120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01309/01/2017
    Labeler - AAA Pharmaceutical, Inc. (181192162)