LOW DOSE ASPIRIN- aspirin tablet, coated 
P & L Development, LLC

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Drug Facts

Active ingredient (in each tablet)

Aspirin 81 mg (NSAID)*

*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:  

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 his 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 are taking a diuretic
  • you have asthma 

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:
    • feel faint
    • vomit blood
    • have bloody or black stool
    • have stomach pain that does not get better
  • pain gets worse or lasts more than 10 days
  • redness or swelling is present 
  • ringing in the ears or loss of hearing occurs
  • 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 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 (1-800-222-1222) right away. 

Directions

Other information

Inactive ingredients

croscarmellose sodium, D&C yellow #10, lactose monohydrate, methacrylic acid copolymer, microcrystalline cellulose 102 polacrilin potassium, polyethylene glycol 6000, polyvinyl alcohol, purified water, talc, silicon dioxide, sodium lauryl sulfate, soybean, titanium dioxide, triethyl citrate

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST 

Principal Display Panel

Compare to the active ingredient in Bayer® Low Dose Aspirin†

EASY OPEN CAP

Low Dose 

Aspirin 81 mg

Pain reliever (NSAID)

≠aspirin regimen

≠safety coated

THIS PACKAGE NOT FOR HOUSEHOLDS WITH YOUNG CHILDREN

enteric coated tablets

≠≠Coating helps protect against stomach upset

†This product is not manufactured or distributed by Bayer HealthCare LLC, distributor of Bayer® Low Dose Aspirin.

≠Talk to your doctor or other healthcare provider before using this product for your heart. Aspirin is not right for everyone.

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

Distributed by:

PL Developments

200 Hicks Street

Westbury, NY 11590

Product Label

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

READYinCASE Low Dose Aspirin 81 mg

LOW DOSE ASPIRIN 
aspirin tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59726-065
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN81 mg
Inactive Ingredients
Ingredient NameStrength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
METHACRYLIC ACID (UNII: 1CS02G8656)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
POLACRILIN POTASSIUM (UNII: 0BZ5A00FQU)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
SOYBEAN (UNII: L7HT8F1ZOD)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
Product Characteristics
ColoryellowScoreno score
ShapeROUNDSize6mm
FlavorImprint Code P
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59726-065-30300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/13/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01308/13/2021
Labeler - P & L Development, LLC (800014821)

Revised: 4/2024
Document Id: 008ee85b-5cac-45a6-a857-a828f8125175
Set id: 0058175f-3474-40c3-a046-6cfaec86d84b
Version: 3
Effective Time: 20240416
 
P & L Development, LLC