Pain reliefchildrens suspension

Ingredients and appearance - Product information

Pain reliefchildrens suspension- Acetaminophen

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 33992-0282
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Acetaminophen ( UNII: 362O9ITL9D)( Acetaminophen - UNII: 362O9ITL9D ) 160 mgin 5 mL

Inactive Ingredients

Ingredient Name Code
Carboxymethylcellulose sodium ( UNII: K679OBS311)
Acesulfame potassium ( UNII: 23OV73Q5G9)
Butylparaben ( UNII: 3QPI1U3FV8)
Cellulose, microcrystalline ( UNII: OP1R32D61U)
Anhydrous citric acid ( UNII: XF417D3PSL)
Fd&c red no. 40 ( UNII: WZB9127XOA)
Glycerin ( UNII: PDC6A3C0OX)
High fructose corn syrup ( UNII: XY6UN3QB6S)
Propylene glycol ( UNII: 6DC9Q167V3)
Water ( UNII: 059QF0KO0R)
Sodium benzoate ( UNII: OJ245FE5EU)
Sorbitol ( UNII: 506T60A25R)
Xanthan gum ( UNII: TTV12P4NEE)

Product Characteristics

Flavor CHERRY

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 33992-0282-4 118mL in 1 BOTTLE, PLASTIC 2016/06/30

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC MONOGRAPH NOT FINAL part343 USA 2016/06/30

Labeler - ASSURED / DOLLAR TREE (Greenbrier International, Inc.)( 610322518)