Label: ACETAMINOPHEN FOR CHILDREN- acetaminophen suppository
- NDC Code(s): 45802-732-30, 45802-732-33
- Packager: Padagis Israel Pharmaceuticals Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 10, 2021
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- Active ingredient (in each rectal suppository)
- Purposes
- Uses
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Warnings
Liver warning:
This product contains acetaminophen. Severe liver damage may occur if your child takes
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- more than 5 doses in 24 hours, which is the maximum daily amount
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- with other drugs containing acetaminophen
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.
For rectal use only
Do not use
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- if you are allergic to acetaminophen
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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.
Ask a doctor before use if
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- your child has liver disease
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- your child is taking the blood thinning drug warfarin
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Directions
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- this product does not contain directions or warnings for adult use
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- do not use more than directed
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- remove wrapper
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- carefully insert suppository well up into the rectum
Dosing Chart
Age
Dose
under 3 years
Do not use unless directed by a doctor
3 to 6 years
Use 1 suppository every 4 to 6 hours (maximum of 5 doses in 24 hours)
- Other information
- Inactive ingredient
- Questions or comments?
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INGREDIENTS AND APPEARANCE
ACETAMINOPHEN FOR CHILDREN
acetaminophen suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:45802-732 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 120 mg Inactive Ingredients Ingredient Name Strength COTTONSEED OIL (UNII: H3E878020N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:45802-732-33 100 in 1 CARTON 12/14/2010 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:45802-732-30 12 in 1 CARTON 03/09/2011 2 1 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 ANDA ANDA070607 12/14/2010 Labeler - Padagis Israel Pharmaceuticals Ltd (600093611)