CHILDRENS SILAPAP LIQUID-GRAPE FLAVOR  - acetaminophen liquid 
Silarx Pharmaceuticals, Inc

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Children's Silapap Liquid-Grape Flavor

Drug Facts

Active ingredient (in each 2.5 mL)     Purpose

Acetaminophen 80 mg                               Pain reliever/fever reducer

Uses

Warnings

When using this product do not use

Stop use and ask a doctor if the child has

Keep out reach of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away

Directions


children under 2 years (under 24 lbs)
ask a doctor
children 2-3 years(24-35 lbs)
1 teaspoonful (5 mL)
children 4-5 years (36-47 lbs)
1 1/2 teaspoonfuls (7.5 mL)
children 6-8 years (48-59 lbs)
2 teaspoonfuls (12.5 mL)
children 9-10 years (60-71 lbs)
2 1/2 teaspoonfuls (12.5)
children 11 years (72-95 lbs)
3 teaspoonfuls (15 mL)
Other information
store at room temperature

Inactive ingredients

artificial grape flavor, citric acid, FD&C Blue #1, FD&C Red #40, methylparaben, propylene glycol, saccharin sodium, sodium benzoate, water

This product is not manufactured or distributed by McNeil Consumer Products., owner of the registered trademark TYLENOL®

Mfg. by:

Silarx Pharmaceuticals, Inc.
Spring Valley, NY 10977


Container Label



CHILDRENS SILAPAP LIQUID-GRAPE FLAVOR 
childrens silapap liquid-grape flavor   liquid
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)54838-118
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (Acetaminophen) Acetaminophen80 mg  in 2.5 mL
Inactive Ingredients
Ingredient NameStrength
anhydrous citric acid 
FD&C blue no. 1 
FD&C red no. 40 
methylparaben 
propylene glycol 
saccharin sodium 
sodium benzoate 
water 
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
154838-118-40118 mL In 1 BOTTLE, PLASTICNone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34109/01/199902/20/2004

Labeler - Silarx Pharmaceuticals, Inc (161630033)
Revised: 06/2009Silarx Pharmaceuticals, Inc