Label: CHILDRENS MAPAP ACETAMINOPHEN- acetaminophen liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 17856-1985-1, 17856-1985-5, 17856-1985-9 - Packager: Atlantic Biologicals Corps
- This is a repackaged label.
- Source NDC Code(s): 0904-1985
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 18, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each TSP (5 mL))
- Purpose
- Uses
-
Warnings
Liver warning
This product contains acetaminophen. Severe liver damage may occur if your child takes:
- more than 5 doses in 24 hours, which is the maximum daily amount
- with other drugs containing acetaminophen
Sore throat warning
If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Do not use
- with any other product containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
Stop use and ask a doctor if
- pain gets worse or last for more than 5 days
- fever gets worse or last for more than 3 days
- new symptoms occur
- redness or swelling is present
These could be signs of a serious condition.
Overdose warning
Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.
-
Directions
- this product does not contain directions or complete warnings for adult use
- find right dose on chart
- if possible, use weight to dose; otherwise, use age
- if needed, repeat dose every 4 hours
- do not use more than 5 doses in 24 hours
Weight Age Dose under 24 lbs Under 2 years ask a doctor 24 to 35 lbs 2 to 3 years 1 TSP (5 mL) 36 to 47 lbs 4 to 5 years 1 1/2 TSP (7.5 mL) 48 to 59 lbs 6 to 8 years 2 TSP (10 mL) 60 to 71 lbs 9 to 10 years 2 1/2 TSP (12.5 mL) 72 to 95 lbs 11 years 3 TSP (15 mL) -
Other information
- sodium 1mg Each TSP(5 mL) contains:
- TAMPER-EVIDENT: Do not use this product if inner foil seal over mouth of the bottle is cut, torn, broken, or missing.
- store at 20° - 25°C (68° – 77°F)
- this product is not the same concentration as Infants' Drops. For accurate dosing, follow the dosing instructions on this label.
- Inactive ingredients
- Questions?
- CHILDRENS MAPAP ACETAMINOPHEN (ACETAMINOPHEN) LIQUID
-
INGREDIENTS AND APPEARANCE
CHILDRENS MAPAP ACETAMINOPHEN
acetaminophen liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17856-1985(NDC:0904-1985) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen 160 mg in 5 mL Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Sorbitol (UNII: 506T60A25R) Sodium Benzoate (UNII: OJ245FE5EU) Anhydrous citric acid (UNII: XF417D3PSL) FD&C Red no. 40 (UNII: WZB9127XOA) Water (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Propylene glycol (UNII: 6DC9Q167V3) PRUNUS SEROTINA BARK (UNII: 5D48E975HA) POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Product Characteristics Color RED Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17856-1985-1 5 mL in 1 CUP; Type 0: Not a Combination Product 07/22/2016 10/18/2019 2 NDC:17856-1985-5 5 mL in 1 CUP; Type 0: Not a Combination Product 07/22/2016 10/18/2019 3 NDC:17856-1985-9 1 mL in 1 SYRINGE; Type 0: Not a Combination Product 10/18/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part343 07/22/2016 Labeler - Atlantic Biologicals Corps (047437707) Registrant - Atlantic Biologicals Corps (047437707) Establishment Name Address ID/FEI Business Operations Atlantic Biologicals Corps 047437707 RELABEL(17856-1985) , REPACK(17856-1985)