ENTERIC COATED ASPIRIN REGULAR STRENGTH- aspirin tablet, delayed release

Enteric Coated Aspirin by

Drug Labeling and Warnings

Enteric Coated Aspirin by is a Otc medication manufactured, distributed, or labeled by Bryant Ranch Prepack. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DO NOT USE

Do not use

• if you are allergic to aspirin or any other pain reliever/fever reducer
  

ASK DOCTOR

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 DOCTOR/PHARMACIST

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

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
  

PREGNANCY OR BREAST FEEDING

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

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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
  

STORAGE AND HANDLING

Other information

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

INACTIVE INGREDIENT

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

INDICATIONS & USAGE

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

PURPOSE

Pain Reliever

WARNINGS

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.

ACTIVE INGREDIENT

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

HOW SUPPLIED

Product: 71335-0157

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

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

NDC: 71335-0157-3 100 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: 71335-0157-6 45 TABLET, DELAYED RELEASE in a BOTTLE

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

Aspirin E.C 325mg Tablet

INGREDIENTS AND APPEARANCE

ENTERIC COATED ASPIRIN   REGULAR STRENGTH
aspirin tablet, delayed release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71335-0157(NDC:49483-331)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E)	ASPIRIN	325 mg

Inactive Ingredients
Ingredient Name	Strength
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MINERAL OIL (UNII: T5L8T28FGP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
DIMETHICONE (UNII: 92RU3N3Y1O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)

Product Characteristics
Color	orange	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	T
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71335-0157-1	30 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013
2	NDC: 71335-0157-2	60 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013
3	NDC: 71335-0157-3	100 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013
4	NDC: 71335-0157-4	90 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013
5	NDC: 71335-0157-5	20 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013
6	NDC: 71335-0157-6	45 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013
7	NDC: 71335-0157-7	120 in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part343	01/04/2011

Labeler - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(71335-0157) , RELABEL(71335-0157)