![WAL-NADOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET [WALGREEN COMPANY]](https://medic.hrt.org//dailymed/images/a4c40c16-7f03-4148-aa57-acf626e0d8cd/walgreens-44-148-1.jpg)
- Active ingredient (in each tablet)
- 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
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Directions
- do not take more than directed
- adults and children 12 years and over
- take 2 tablets every 6 hours while symptoms persists or as directed by a doctor
- do not take more than 6 tablets in 24 hours, unless directed by a doctor
- do not take for more than 10 days unless directed by a doctor
- children under 12 years: ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Walgreens
Compare to Panadol® Extra Strength
Tablets active ingredient††
NDC 0363-0148-01
Wal-Nadol
ACETAMINOPHEN 500 mg / PAIN RELIEVER / FEVER REDUCEREXTRA STRENGTH TABLETS
30 TABLETS
TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSINGWalgreens Pharmacist Survey
††This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare, owner of the registered trademark Panadol® Extra Strength Tablets.
50844 ORG071814801
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com ©2018 Walgreen Co.
Walgreens 44-148
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INGREDIENTS AND APPEARANCE
WAL-NADOL EXTRA STRENGTH
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0148 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 POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STEARIC ACID (UNII: 4ELV7Z65AP) STARCH, CORN (UNII: O8232NY3SJ) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) Product Characteristics Color WHITE Score 2 pieces Shape ROUND Size 12mm Flavor Imprint Code 44;148 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0148-01 1 in 1 CARTON 01/21/1993 1 30 in 1 BOTTLE; 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 01/21/1993 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 PACK(0363-0148) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 MANUFACTURE(0363-0148) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 PACK(0363-0148) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 PACK(0363-0148)