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Target Corporation

Target Corporation Aspirin Tablets, 81 mg Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Aspirin 81 mg (NSAID)*

*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever

up and up aspirin Uses

  • temporarily relieves minor aches and pains

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 use

if you have ever had an allergic reaction to 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 are

  • taking a prescription drug for diabetes, gout 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 for more than 10 days
  • redness or swelling is present
  • any new symptoms appear
  • ringing in the ears or loss of hearing occurs

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 right away. (1-800-222-1222)

Directions

  • drink a full glass of water with each dose
adults and children 12 years and over
  • take 4 to 8 tablets every 4 hours while symptoms persist
  • do not exceed 48 tablets in 24 hours or as directed by a doctor
children under 12 years
  • do not use unless directed by a doctor

up and up aspirin Other information

store at 20º-25ºC (68º-77ºF)

Inactive ingredients

carnauba wax, colloidal silicon dioxide, croscarmellose sodium, edible ink, FD&C red no. 3, FD&C red no. 40, FD&C yellow no. 6, hypromellose, methacrylic acid copolymer, microcrystalline cellulose, pregelatinized starch, sodium bicarbonate, sodium lauryl sulfate, stearic acid, talc, titanium dioxide, triacetin, triethyl citrate

Questions?

Call 1-800-910-6874

Principal Display Panel

Aspirin Tablets, 81 mg

Pain Reliever (NSAID)

Compare to active ingredient in St.Joseph® 81 mg

See New Warnings Information

Adult Low-Strength

Aspirin Regimen

# Tablets {Replace "#" with the number of tablets in the container}

Shown Actual Size Above

up and up aspirin
Aspirin Tablets, 81 mg Carton Image 1 Aspirin Tablets, 81 mg Carton Image 2

up and up aspirin

Aspirin TABLET, FILM COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-277
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
aspirin ASPIRIN 81 mg

Inactive Ingredients

Ingredient Name Strength
carnauba wax
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
FD&C RED NO. 3
FD&C RED NO. 40
FD&C YELLOW NO. 6
HYPROMELLOSES
cellulose, microcrystalline
SODIUM BICARBONATE
SODIUM LAURYL SULFATE
STEARIC ACID
talc
titanium dioxide
triacetin
TRIETHYL CITRATE

Product Characteristics

Color Size Imprint Code Shape
ORANGE (peach) 8 mm L277 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 180 in 1 BOTTLE
2 NDC:11673-277-48 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2009-07-22


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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