Label: ASPIRIN LOW DOSE- aspirin tablet, delayed release
- NDC Code(s): 17856-3086-1
- Packager: ATLANTIC BIOLOGICALS CORP.
- This is a repackaged label.
- Source NDC Code(s): 0536-1234
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 19, 2025
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Active ingredient (in each tablet)
Aspirin 81 mg (NSAID)* *nonsteroidal anti-inflammatory drug
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Purpose
Pain reliever
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Description
NDC 17856-3086-01 - Talk to your doctor or other healthcare provider before using this product for your heart. Low Dose - Aspirin 81 mg - Safety Coated - Pain Reliever (NSAID) Aspirin Regimen - 100 ...
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Uses
for the temporary relief of minor aches and pains or as recommended by your doctor. Because of its delayed action, this product will not provide fast relief of headaches or other symptoms ...
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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 ...
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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 not to exceed 48 tablets in 24 hours unless directed by a doctor ...
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Other information
store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) see end flap for expiration date and lot number
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Inactive ingredients
corn starch, D&C yellow #10, FD&C yellow #6, hypromellose, methacrylic acid, microcrystalline cellulose, polydextrose, polyethylene glycol, shellac wax, silica, simethicone, sodium bicarbonate ...
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DISTRIBUTED BY: ATLANTIC BIOLOGICALS CORP. MIAMI, FL 33179
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