Low Dose Aspirin
FDA Label NDC 68210-5029
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Spirit Pharmaceuticals Llc for the product Low Dose Aspirin (NDC 68210-5029). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet) aspirin 81 mg (nsaid)nonsterodial anti-inflammatory drug, purpose pain reliever, ask a doctor or pharmacist before use if you are ask a doctor or pharmacist before use if you are taking a prescription drug for:gout, diabetes, arthritis, keep out of reach of children in case of overdose, get medical help or contact poison control center right away., directions, other information, inactive ingredients, questions or comments, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose Pain Reliever
Ask A Doctor Or Pharmacist Before Use If You Are Ask A Doctor Or Pharmacist Before Use If You Are Taking A Prescription Drug For:Gout, Diabetes, Arthritis
Keep Out Of Reach Of Children In Case Of Overdose, Get Medical Help Or Contact Poison Control Center Right Away.
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
Other Information
Store at room temparature. Avoid excessive heat above 40°C (104 °F)
Inactive Ingredients
acrycoat, colloidal silicon dioxide, croscarmellose sodium, D&C yellow # 10, Lactose, microcrystalline cellulose, polysorbate 80,
sodium hydroxide, talc, titanium dioxide, triethyl citrate, yellow oxide of iron
Questions Or Comments
1-888-333-9792
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