Label: ASPIRIN tablet, coated
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Contains inactivated NDC Code(s)
NDC Code(s): 52204-103-99 - Packager: Cispharma, Inc
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated April 17, 2011
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- Official Label (Printer Friendly)
- Drug Facts
- PURPOSE
- Uses
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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:
- facial swelling
- asthma (wheezing)
- shock
- hives
Alcohol Warning: if you consume 3 or more alcoholic drinks every day, ask your doctor whether you should take aspirin or other pain relievers/fever reducers. Aspirin may cause stomach bleeding.
Ask a doctor before use if you have
- stomach problems (such as heartburn, upset stomach, or stomach pain) that last or come back
- bleeding problems
- ulcers
- asthma
Ask a doctor or pharmacist before use if you are taking a prescription drug for
- diabetes
- gout
- arthritis
- anticoagulation ( thinning of blood)
Stop use and ask a doctor if
- An allergic reaction occurs. Seek medical help right away
- Pain gets worse or lasts more than 10 days
- Redness or swelling is present
- New symptoms occur
- Ringing in the ears or loss of hearing occurs.
- OVERDOSAGE
- Directions:
- Other Information
- Inactive Ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ASPIRIN
aspirin tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52204-103 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 81 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 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 WAX (UNII: XOF597Q3KY) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) Product Characteristics Color YELLOW (YELLOW) Score no score Shape ROUND (Round) Size 6mm Flavor Imprint Code C;3 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52204-103-99 166667 in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part343 02/14/2011 Labeler - Cispharma, Inc (833171445) Registrant - Cispharma, Inc (833171445) Establishment Name Address ID/FEI Business Operations Cispharma, Inc 833171445 manufacture