Label: ASPIRIN 81 MG- aspirin enteric coated tablets 81 mg tablet, delayed release
- NDC Code(s): 55681-402-03
- Packager: TWIN MED LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 12, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INACTIVE INGREDIENT
- ACTIVE INGREDIENT
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- Aspirin Drug Facts
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- PURPOSE
- STOP USE
- DOSAGE & ADMINISTRATION
- WARNINGS
- SPL UNCLASSIFIED SECTION
- OTHER SAFETY INFORMATION
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ASPIRIN 81 MG
aspirin enteric coated tablets 81 mg tablet, delayed releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55681-402 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 STEARIC ACID (UNII: 4ELV7Z65AP) POVIDONE (UNII: FZ989GH94E) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) SODIUM LAURYL SULFATE (UNII: 368GB5141J) MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:2) (UNII: XRK36F13ZZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM BICARBONATE (UNII: 8MDF5V39QO) TALC (UNII: 7SEV7J4R1U) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Product Characteristics Color yellow Score no score Shape ROUND Size 8mm Flavor Imprint Code S17 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55681-402-03 300 in 1 BOTTLE; Type 0: Not a Combination Product 11/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 11/01/2022 Labeler - TWIN MED LLC (009579330)