ASPIRIN 81- aspirin tablet, delayed release 
Amerisource Bergen

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Good Neighbor Pharmacy 44-645

Active ingredient (in each tablet)

Aspirin 81 mg (NSAID)*
*nonsteroidal anti-inflammatory drug 

Purpose

Pain reliever 

Uses

for the temporary relief of minor aches and pains or as recommended by your doctor. Because of its delayed action, this product will not provide fast relief of headaches or other symptoms needing immediate relief.

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:

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

Do not use

  • if you are allergic to aspirin or any other pain reliever/fever reducer
  • if you have ever had an allergic reaction to this product or any of its ingredients

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 have asthma
  • you are taking a diuretic

Ask a doctor or pharmacist before use if you are

taking a prescription drug for

  • gout
  • diabetes
  • 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:
    • vomit blood
    • have bloody or black stools
    • feel faint
    • have stomach pain that does not get better
  • ringing in the ears or a loss of hearing occurs
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • 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 at 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, corn starch, FD&C red #40, FD&C yellow #6, hypromellose, methacrylic acid, microcrystalline cellulose, polydextrose, polyethylene glycol, shellac wax, simethicone, sodium bicarbonate, sodium lauryl sulfate, talc, titanium dioxide, triacetin, triethyl citrate


Questions or comments?

1-800-426-9391 

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Good
Neighbor
Pharmacy
®

Compare to St. Joseph® Low Dose Safety Coated
81 mg Aspirin active ingredient**

NDC 46122-598-48

LOW DOSE

Aspirin 81 mg
Pain Reliever (NSAID)

Enteric Coated

180 Tablets | 81 mg Each

Actual
Size

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

**This product is not manufactured or
distributed by Foundation Consumer
Healthcare, LLC, owner of the registered
trademark St. Joseph® Low Dose Safety
Coated 81 mg Aspirin.

50844   REV0122B64560

Distributed By
AmerisourceBergen
1 West First Avenue
Conshohocken, PA 19428
Questions or Concerns?
www.mygnp.com

GOOD NEIGHBOR PHARMACY
SATISFACTION
GUARANTEED
BRAND PRODUCTS

Good Neighbor Pharmacy 44-645

Good Neighbor Pharmacy 44-645

ASPIRIN 81 
aspirin tablet, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-598
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN81 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
METHACRYLIC ACID (UNII: 1CS02G8656)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SHELLAC (UNII: 46N107B71O)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
WATER (UNII: 059QF0KO0R)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
Product Characteristics
ColorpinkScoreno score
ShapeROUNDSize6mm
FlavorImprint Code L
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-598-481 in 1 CARTON05/31/2019
1180 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:46122-598-87300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/31/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01305/31/2019
Labeler - Amerisource Bergen (007914906)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(46122-598)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(46122-598)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(46122-598)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(46122-598)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(46122-598)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.117025878manufacture(46122-598)

Revised: 7/2023
Document Id: 7c0131ad-9ccf-40d2-aa19-e67f325fd92a
Set id: 4491faca-f30b-4eb0-bea9-f518f6b2f095
Version: 8
Effective Time: 20230722
 
Amerisource Bergen