Label: ST. JOSEPH LOW DOSE ASPIRIN- aspirin tablet, film coated
-
NDC Code(s):
69536-181-12,
69536-181-15,
69536-181-20,
69536-181-36, view more69536-181-54, 69536-181-65
- Packager: Foundation Consumer Healthcare
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 26, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
-
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
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 aretaking a prescription drug for gout, diabetes or arthritis
Stop use and ask a doctor if
- an allergic reaction occurs. Seek medical help right away.
- you experience any of the following signs of stomach bleeding:
- feel faint
- vomit blood
- have bloody or black stools
- have stomach pain that does not get better
- pain gets worse or lasts more than 10 days
- ringing in the ears or loss of hearing occurs
- redness or swelling is present
- new symptoms occur. These could be signs of a serious condition.
- Directions
- Other information
-
Inactive ingredients
colloidal anhydrous silica, FD&C red #40, FD&C yellow #6, hypromellose, methacrylic acid- ethyl acrylate copolymer, microcrystalline cellulose, polydextrose, polyethylene glycol, pregelatinized starch, shellac wax, simethicone, sodium bicarbonate, sodium lauryl sulfate, talc, titanium dioxide, triacetin, triethyl citrate
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 36 Tablet Bottle Box
-
INGREDIENTS AND APPEARANCE
ST. JOSEPH LOW DOSE ASPIRIN
aspirin tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69536-181 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 81 mg Inactive Ingredients Ingredient Name Strength FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) METHACRYLIC ACID (UNII: 1CS02G8656) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SODIUM LAURYL SULFATE (UNII: 368GB5141J) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) TRIACETIN (UNII: XHX3C3X673) POLYDEXTROSE (UNII: VH2XOU12IE) SHELLAC (UNII: 46N107B71O) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Product Characteristics Color white (PEACH) Score no score Shape ROUND Size 7mm Flavor Imprint Code SJ Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69536-181-15 1 in 1 BOX 02/17/2017 1 150 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69536-181-36 1 in 1 BOX 02/17/2017 2 36 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:69536-181-12 1 in 1 BOX 02/17/2017 3 120 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:69536-181-20 1 in 1 BOX 02/17/2017 4 200 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:69536-181-54 1 in 1 BOX 02/17/2017 05/01/2018 5 54 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:69536-181-65 1 in 1 BOX 02/17/2017 6 365 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 02/17/2017 Labeler - Foundation Consumer Healthcare (079675882)