NDC | 67414-449-00, 67414-449-10, 67414-449-11 |
Set ID | fba711c1-4e69-49b0-8994-97c455aebcb2 |
Category | HUMAN OTC DRUG LABEL |
Packager | Jones Packaging Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART343 |
- Active ingredient (in each caplet)
- Uses
-
Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take • more than 4,000 mg of acetaminophen in 24 hours
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product. Allergy alert: acetaminophen may cause severe skin reactions.symptoms may include:
- skin reddening
- blisters
- rash if a skin reaction occurs. stop use and seek medical help right away.
Do not use
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen. ask a doctor or pharmacist.
- if you are allergic to acetaminophen or any of the inactive ingredients in this product.
-
Directions
- do not take more than directed (see overdose warning).
Adults and children 12 years and over: - take 2 capletes every 6 hours while symptoms last
- do not take more than 6 capletes in 24 hours, unless directed by a doctor
- do not use for more than 10 days unless directed by a doctor
children under 12 years ask a doctor - Other information
- Inactive ingredients
- Questions or comments?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
TYLENOL EXTRA STRENGTH CAPLET
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67414-449 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg Inactive Ingredients Ingredient Name Strength CARNAUBA WAX (UNII: R12CBM0EIZ) STARCH, CORN (UNII: O8232NY3SJ) FD&C RED NO. 40 (UNII: WZB9127XOA) ALUMINUM OXIDE (UNII: LMI26O6933) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SHELLAC (UNII: 46N107B71O) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white Score no score Shape OVAL Size 18mm Flavor Imprint Code TYLENOL500 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67414-449-00 2500 in 1 BOX 01/24/2018 1 2 in 1 POUCH; Type 0: Not a Combination Product 2 NDC:67414-449-10 50 in 1 BOX 01/24/2018 2 2 in 1 POUCH; Type 0: Not a Combination Product 3 NDC:67414-449-11 50 in 1 BOX 01/24/2018 3 2 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part343 01/24/2018 Labeler - Jones Packaging Inc (243697187) Registrant - Jones Packaging Inc (243697187) Establishment Name Address ID/FEI Business Operations Jones Packaging Inc 243697187 pack(67414-449) Establishment Name Address ID/FEI Business Operations Dr. Reddy's Laboratories Louisiana, LLC 830397282 manufacture(67414-449) Establishment Name Address ID/FEI Business Operations McNeil Healthcare LLC. 831188763 manufacture(67414-449)