CHILDREN ACETAMINOPHEN ORAL SOLUTION- acetaminophen liquid 
MAJOR PHARMACEUTICALS

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Major- APAP Child Sol 7014

Active ingredient (per 5 mL teaspoonful)

Acetaminophen 160 mg

Purpose

Pain Reliever/Fever Reducer

Warnings

Liver Warning: This product contains acetaminophen. Severe liver damage may occur if your child takes:

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: if sore thoat 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

Ask a doctor before use if your child has liver disease.

Ask a doctor before use if your child is taking the blood thinning drug warfarin.

When using this product: Do not exceed recommended dose.

Stop use and ask a doctor if

Uses

If pregnant or breast-feeding, ask a health professional before use

Keep out of reach of children. In case of overdose, get medical help or contact a Paoison Control Center right away. Quick medical attention is critical for adults/children even if you do not notice any signs or symptoms.

Directions

Weight (lbs) under 24 24-35 36-4748-59 60-71 72-95
Age (years) under 2 2 to 3 4 to 5 6 to 8 9 to 10 11
Dosage Teaspoonful (tsp) consult Physician 1 tsp (5 mL) 1 1/2 tsp (7.5 mL) 2 tsp (10 mL) 2 1/2 tsp (12.5 mL) 3 tsp (15 mL)

Inactive ingredients: artificial and natural cherry flavor, citric acid, FD&C Red #40, methylparaben, polyethylene glycol, propylene glycol, propylparaben, purified water, sodium citrate, sucralose

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CHILDREN ACETAMINOPHEN ORAL SOLUTION 
acetaminophen liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0904-7014
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN160 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0904-7014-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2019
2NDC:0904-7014-20118 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01310/01/2019
Labeler - MAJOR PHARMACEUTICALS (191427277)

Revised: 6/2025
Document Id: 372893a0-1ef9-1c7c-e063-6294a90a6181
Set id: cfca5147-f390-40bd-8f13-c5b3b8d1c5b0
Version: 7
Effective Time: 20250609
 
MAJOR PHARMACEUTICALS