CHILDRENS PAIN AND FEVER- acetaminophen liquid 
Marc Glassman, Inc.

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 Facts
Active ingredient

Active ingredient

(in each 5 mL = 1 teaspoonful)

Acetaminophen 160 mg

Purpose

Pain reliver/fever reducer

Keep out of reach of children.

Keep out of reach of children.

Uses

temporarily reduces

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

Allergy alert
Acetaminophen may cause severe skin reactions.
Symptoms may include: ■ skin reddening ■ blisters
■ rash. If skin reaction occurs, stop use and seek
medical help right away

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

Ask a doctor before use if your child has

liver disease

Ask a doctor or pharmacist before use if your child is

taking the blood thinning drug warfarin.

When using this product do not exceed recommended dose (see overdose warning)
Stop use and ask a doctor if

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 right awway. (1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

 Weight (lb) Age (yr) Dose (mL or tsp)*
 under 24 under 2 years ask a doctor
 24-35 2-3 years 5 mL (1 tsp)
 36-47 4-5 years 7.5 mL (1 1/2 tsp)
 48-59 6-8 years 10 mL (2 tsp)
 60-71 9-10 years 12.5 mL (2 1/2 tsp)
 72-95 11 years 15 mL (3 tsp)

* or use as directed

Attention: use only enclosed dosing cup specifically designed for use with this product. Do not use any other dosing device.

Other information

Inactive ingredients

anhydrous citric acid, butylparaben, FD and C red # 40, flavor, glycerin, high fructose corn syrup, microcrystalline cellulose and carboxymethylcellulose sodium, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose, xanthan gum

Marcs Childrens Pain and Fever Product Label

NDC 68998-525-24

Compare to the active ingredient in childrens Tylenol® oral suspension*

MARCS

Childrens

Pain and Fever

Pain Reliver / Fever Reducer

Acetaminophen Oral Suspension

For Ages 2 to 11

CHERRY FLAVOR

4 FL OZ (118 mL)

160 mg per 5 mL

DO NOT USE IF PRINTED NECKBAND IS BROKEN OR MISSING

* This product is not manufactured or distributed by McNeil Consumer Healthcare, Distributer of Childrens Tylenol® Oral Suspension

Distributed by:

Marc Glassman, Inc.

West 130th Street

Cleveland, OH 44130

BX-045

LR-076

Lot:

Exp:

68993-524 118mL bottle

68993-524 118mL box

rres

CHILDRENS PAIN AND FEVER 
acetaminophen liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68998-525
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)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68998-525-24118 mL in 1 BOTTLE; Type 0: Not a Combination Product10/10/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34310/10/2014
Labeler - Marc Glassman, Inc. (094487477)

Revised: 12/2020
Document Id: ef7d4b51-91de-4d46-83e0-91ec211f44f5
Set id: f708e1ec-cf2a-4e2b-851f-f6b703f359b2
Version: 3
Effective Time: 20201231
 
Marc Glassman, Inc.