NDC | 50580-378-01, 50580-378-02, 50580-378-03 |
Set ID | 17cfa99d-abb2-4d77-9e0e-e77109fbb61a |
Category | HUMAN OTC DRUG LABEL |
Packager | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART343 |
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each caplet)
- Purpose
- Uses
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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 caplets every 6 hours while symptoms last
- do not take more than 6 caplets 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?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TYLENOL EXTRA STRENGTH
acetaminophen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50580-378 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) CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK) FD&C red no. 40 (UNII: WZB9127XOA) aluminum oxide (UNII: LMI26O6933) hypromellose, unspecified (UNII: 3NXW29V3WO) magnesium stearate (UNII: 70097M6I30) microcrystalline cellulose (UNII: OP1R32D61U) polyethylene glycol, unspecified (UNII: 3WJQ0SDW1A) polysorbate 80 (UNII: 6OZP39ZG8H) povidone, unspecified (UNII: FZ989GH94E) propylene glycol (UNII: 6DC9Q167V3) shellac (UNII: 46N107B71O) sodium starch glycolate type A potato (UNII: 5856J3G2A2) stearic acid (UNII: 4ELV7Z65AP) titanium dioxide (UNII: 15FIX9V2JP) Product Characteristics Color WHITE Score no score Shape OVAL Size 19mm Flavor Imprint Code TYLENOL;500 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50580-378-01 1 in 1 CARTON 11/01/2014 1 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:50580-378-02 1 in 1 CARTON 11/01/2014 2 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:50580-378-03 225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/06/2015 4 NDC:50580-378-04 1 in 1 CARTON 03/01/2021 4 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 5 NDC:50580-378-05 1 in 1 CARTON 03/01/2021 5 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 6 NDC:50580-378-06 1 in 1 CARTON 03/01/2021 6 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 7 NDC:50580-378-07 1 in 1 CARTON 03/01/2021 7 225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 8 NDC:50580-378-08 325 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part343 11/01/2014 Labeler - Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division (878046358)