ST. JOSEPH LOW DOSE ASPIRIN- aspirin tablet, film coated 
Foundation Consumer Healthcare

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St. Joseph Low Dose Aspirin

Drug Facts

Active ingredient (in each tablet)

Aspirin 81 mg (NSAID) 1


1
nonsteroidal anti-inflammatory drug

Purpose

Pain reliever

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

Do not useif 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 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.

If pregnant or breast-feeding,ask a health professional before use. It is especially important not to use aspirin 20 weeks or later in 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.

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?

Call 1-855-785-6381weekdays 9 AM to 5 PM EST

Dist. by: Foundation Consumer Healthcare, LLC.
Pittsburgh, PA 15205

PRINCIPAL DISPLAY PANEL - 36 Tablet Bottle Box

•ADULT ASPIRIN REGIMEN

ST. JOSEPH ®

LOW DOSE ASPIRIN
SAFETY COATED
PAIN RELIEVER (NSAID)

81mg

AMERICA'S
ASPIRIN

100
YEARS

DOCTOR RECOMMENDED

Enteric
Coated

36
Coated
Tablets

PRINCIPAL DISPLAY PANEL - 36 Tablet Bottle Box
ST. JOSEPH LOW DOSE ASPIRIN 
aspirin tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69536-181
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN81 mg
Inactive Ingredients
Ingredient NameStrength
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
Colorwhite (PEACH) Scoreno score
ShapeROUNDSize7mm
FlavorImprint Code SJ
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69536-181-151 in 1 BOX02/17/2017
1150 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69536-181-361 in 1 BOX02/17/2017
236 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:69536-181-121 in 1 BOX02/17/2017
3120 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:69536-181-201 in 1 BOX02/17/2017
4200 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:69536-181-541 in 1 BOX02/17/201705/01/2018
554 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:69536-181-651 in 1 BOX02/17/2017
6365 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01302/17/2017
Labeler - Foundation Consumer Healthcare (079675882)

Revised: 4/2024
Document Id: 1705ba3b-36e3-df62-e063-6394a90ab583
Set id: dbf40c7b-ce30-46f0-9dea-2ca8ff1c9f6f
Version: 7
Effective Time: 20240426
 
Foundation Consumer Healthcare