Label: ACETAMINOPHEN tablet
- NDC Code(s): 55154-7899-0
- Packager: Cardinal Health 107, LLC
- This is a repackaged label.
- Source NDC Code(s): 0904-6773
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 23, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- PURPOSE
- Uses
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WARNINGS
Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. Severe liver damage may occur if
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- adult takes more than 4,000 mg of acetaminophen in 24 hours
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- child takes more than 5 doses in 24 hours, which is the maximum daily amount
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- taken with other drugs containing acetaminophen
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- adult has 3 or more alcoholic drinks every day while using this product
Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:
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- skin reddening
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- blisters
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- rash
If a skin reaction occurs, stop use and seek medical help right away.
Do not use
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- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
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- if you are allergic to acetaminophen or any of the inactive ingredients in this product
Stop use and ask a doctor if
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- pain gets worse or lasts more than 10 days in adults
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- pain gets worse or lasts more than 5 days in children under 12 years
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- fever gets worse or lasts more than 3 days
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- new symptoms occur
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- redness or swelling is present
These could be signs of a serious condition.
Overdose warning
In case of overdose, get medical help or contact a Poison Control Center right away.(1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. This Unit Dose package is not child
resistant and is Intended for Institutional Use Only.
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Directions
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- do not take more than directed (see overdose warning)
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- adults and children 12 years and over:
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- take 2 tablets every 4 to 6 hours while symptoms last
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- do not take more than 10 tablets in 24 hours, unless directed by a doctor
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- do not use for more than 10 days unless directed by a doctor
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children 6 years to under 12 years
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- take 1 tablet every 4 to 6 hours while symptoms last
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- do not take more than 5 tablets in 24 hours
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- do not use for more than 5 days unless directed by a doctor
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- children under 6 years: ask a doctor
- Other information
- INACTIVE INGREDIENT
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
ACETAMINOPHEN
acetaminophen tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55154-7899(NDC:0904-6773) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg Inactive Ingredients Ingredient Name Strength STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) STARCH, CORN (UNII: O8232NY3SJ) POVIDONE K30 (UNII: U725QWY32X) Product Characteristics Color white Score 2 pieces Shape ROUND Size 10mm Flavor Imprint Code CPC;220 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55154-7899-0 1 in 1 BAG 10/23/2018 1 10 in 1 BLISTER PACK; 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 10/23/2018 Labeler - Cardinal Health 107, LLC (118546603)
