Enteric Coated Aspirin Tablet, Delayed Release
Product Images NDC 49483-331

This appears to be a drug label for a pain reliever containing 325mg of aspirin as the active ingredient. It is indicated for use to temporarily relieve minor aches and pains, including headache, toothache, menstrual pain, and minor arthritis pain. It is also indicated for use as a fever reducer. The drug is recommended for use in adults and children over 12 years old. It is recommended to be taken with water, and the maximum dose is 12 tablets in a 24-hour period. There is a warning to consult a doctor before use if the patient has a history of stomach problems, high blood pressure, or kidney disease. Additionally, patients who are recovering from chickenpox or flu-like symptoms should not use this drug. There is also a warning that aspirin may cause a severe allergic reaction. The inactive ingredients are listed as croscarmellose, aluminum lake, hypromellose, methacrylic acid, and ethyl. It is advised to not use this product if the package's foil seal over the mouth of the bottle is cut, torn, broken, or missing. If someone accidentally takes more than the recommended dosage, they should contact a poison control center.*

This is a bulk shipment of aspirin delayed release tablets manufactured by Time-Cap Labs Inc, with a theoretical quantity of 9999777727, and containing 777 CTNs of 997 CTNs. The tablets are enteric-coated with an embossed "T" and should be stored at temperatures between 15°-80°C. The product is intended for manufacturing, processing, or repackaging and should be repacked and labeled immediately upon receipt to comply with applicable regulations of the Food, Drug and Cosmetic Act. The packaging specifications can be obtained from Time-Cap Labs upon request, and their responsibility ceases upon removal of the product from the bulk containers or failure to comply with their packaging and/or labeling specifications. The shipment was sent to the address: 227722272727229297072072202207072277279220722222072220292772227772.*