Label: PAIN RELIEVER EXTRA STRENGTH- acetaminophen tablet, film coated
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NDC Code(s):
0363-0175-03,
0363-0175-08,
0363-0175-12,
0363-0175-14, view more0363-0175-15, 0363-0175-20, 0363-0175-29, 0363-0175-37, 0363-0175-57, 0363-0175-99
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 3, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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:
- rash
- skin reddening
- blisters
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
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Walgreens
Compare to the active ingredient in
Tylenol® Extra Strength Caplets††NDC 0363-0175-03
Pain Reliever
ACETAMINOPHEN 500 mg
PAIN RELIEVER/FEVER REDUCERExtra Strength
10 CAPLETS
ACTUAL SIZE
OPEN HERE TO VIEW COMPLETE PRODUCT INFORMATION
TAMPER EVIDENT: DO NOT USE IF PRINTED
TEAR STRIP IS BROKEN OR MISSINGWalgreens Pharmacist Recommended.
Our pharmacists recommend the Walgreens brand.
We invite you to compare to national brands.††This product is not manufactured or distributed by
Kenvue Inc., owner of the registered trademark Tylenol® Extra Strength Caplets.DISTRIBUTED BY: WALGREEN CO.
DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com ©2021 Walgreen Co.50844
REV0621A17503
Walgreens 44-175
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INGREDIENTS AND APPEARANCE
PAIN RELIEVER EXTRA STRENGTH
acetaminophen tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0175 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 CASTOR OIL (UNII: D5340Y2I9G) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape OVAL Size 17mm Flavor Imprint Code 44;175 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0175-03 10 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/1993 2 NDC:0363-0175-08 1 in 1 CARTON 04/02/1993 04/11/2024 2 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:0363-0175-15 1 in 1 CARTON 04/02/1993 03/16/2024 3 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:0363-0175-12 1 in 1 CARTON 04/02/1993 12/09/2024 4 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 5 NDC:0363-0175-29 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/1993 07/21/2024 6 NDC:0363-0175-20 1 in 1 CARTON 04/02/1993 02/07/2024 6 225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 7 NDC:0363-0175-14 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/1993 02/25/2024 8 NDC:0363-0175-99 1 in 1 CARTON 04/02/1993 02/15/2022 8 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 9 NDC:0363-0175-37 1 in 1 CARTON 04/02/1993 02/07/2021 9 75 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10 NDC:0363-0175-57 1 in 1 CARTON 04/02/1993 02/07/2021 10 125 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M013 04/02/1993 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(0363-0175) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(0363-0175) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(0363-0175) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(0363-0175) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(0363-0175) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117597853 pack(0363-0175)