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← See all Enteric Coated Aspirin Regular Strength brands

Enteric Coated Aspirin Regular Strength

Dosage form: tablet, delayed release
Ingredients: ASPIRIN 325mg
Labeler: Bryant Ranch Prepack
NDC Code: 71335-0157

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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
  • you have not been drinking fluids

Ask a doctor or pharmacist before use if you are
  • taking a prescription drug for diabetes, gout, or arthritis
  • taking any other drug
  • under a doctor's care for any serious condition

Stop use and ask a doctor if
  • you experience any of the following signs of stomach bleeding
    • feel faint
    • have bloody or black stools
    • vomit blood
    • have stomach pain that does not get better
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present in the painful area
  • any new symptoms appear
  • ringing in the ears or a loss of hearing occurs

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.

Directions
  • drink a full glass of water with each dose
  • adults and children 12 years and over: take 1 to 2 tablets every 4 hours while symptoms last. Do not take more than 12 tablets in 24 hours unless directed by a doctor
  • children under 12 years: consult a doctor

Other information
  • store at 25° C (77° F) excursions permitted between 15°-30° C (59°-86° F)
  • use by expiration date on package

corn starch, croscarmellose sodium,D-C yellow #10 aluminum lake, FD-C yellow#6 aluminum lake, hypromellose, methacrylic acid copolymer, microcrystalline cellulose,mineral oil,  polysorbate 80, simethicone, sodium hydroxide, sodium lauryl sulfate, talc, titanium dioxide, triethyl citrate

Use for the temporary relief of minor aches and pains due to:

headache, colds, muscle pain, menstrual pain, toothache, minor pain of arthritis or as directed by your doctor

Pain Reliever

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, shock, asthmaaa9wheezing)

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.

In each Tablet Asprin 325 mg (NSAID*) *non-steroidal anti-inflammatory drug

HOW SUPPLIED

Product: 71335-0157

NDC: 71335-0157-3 100 TABLET, DELAYED RELEASE in a BOTTLE

NDC: 71335-0157-6 45 TABLET, DELAYED RELEASE in a BOTTLE

NDC: 71335-0157-1 30 TABLET, DELAYED RELEASE in a BOTTLE

NDC: 71335-0157-7 120 TABLET, DELAYED RELEASE in a BOTTLE

NDC: 71335-0157-4 90 TABLET, DELAYED RELEASE in a BOTTLE

NDC: 71335-0157-5 20 TABLET, DELAYED RELEASE in a BOTTLE

NDC: 71335-0157-2 60 TABLET, DELAYED RELEASE in a BOTTLE

Aspirin E.C 325mg Tablet
ENTERIC COATED ASPIRIN   REGULAR STRENGTH
aspirin tablet, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-0157(NDC:49483-331)
Route of AdministrationORALDEA ScheduleCIV    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (ASPIRIN) ASPIRIN325 mg  in 325 
Inactive Ingredients
Ingredient NameStrength
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) 
CROSCARMELLOSE SODIUM 
D&C YELLOW NO. 10 
FD&C YELLOW NO. 6 
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A 
MICROCRYSTALLINE CELLULOSE 
MINERAL OIL 
POLYSORBATE 80 
DIMETHICONE 
SILICON DIOXIDE 
SODIUM HYDROXIDE 
SODIUM LAURYL SULFATE 
TALC 
TITANIUM DIOXIDE 
TRIETHYL CITRATE 
HYPROMELLOSE, UNSPECIFIED 
Product Characteristics
ColororangeScoreno score
ShapeROUNDSize11mm
FlavorImprint CodeT
Contains    
Packaging
#Item CodePackage Description
1NDC:71335-0157-3100 TABLET, DELAYED RELEASE in 1 BOTTLE
2NDC:71335-0157-645 TABLET, DELAYED RELEASE in 1 BOTTLE
3NDC:71335-0157-130 TABLET, DELAYED RELEASE in 1 BOTTLE
4NDC:71335-0157-7120 TABLET, DELAYED RELEASE in 1 BOTTLE
5NDC:71335-0157-490 TABLET, DELAYED RELEASE in 1 BOTTLE
6NDC:71335-0157-520 TABLET, DELAYED RELEASE in 1 BOTTLE
7NDC:71335-0157-260 TABLET, DELAYED RELEASE in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34301/04/2011
Labeler - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIOperations
Bryant Ranch Prepack171714327REPACK(71335-0157), RELABEL(71335-0157)

 
Bryant Ranch Prepack

← See all Enteric Coated Aspirin Regular Strength brands

Medically reviewed on Jan 1, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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