CHILDRENS CHEST CONGESTION RELIEF - guaifenesin liquid 
Chain Drug Consortium, LLC

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.

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Active ingredient

Drug Facts

Active ingredient (in each 5 mL teaspoonful)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Keep out of reach of children

Keep out of reach of children.

 In case of overdose, get medical help or contact a Poison Control center right away.

Uses

Warnings

Ask a doctor before use if the child has:


Stop use and ask a doctor if

Directions

AptaPharmaPV ChildCCRelief1 Label

Other information

Inactive ingredients

citric acid anhydrous, dextrose, FD and C Blue # 1, FD and C Red # 40, flavors, glycerin, maltitol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sucralose, xanthan gum

Questions?

Call weekdays from 9:30 AM to 4:30 PM EST

1-877-798-5944

Product Label

NDC 68016-157-04
*COMPARE TO THE ACTIVE INGREDIENTS IN CHILDRENS MUCINEX® CHEST CONGESTION

Premier Value®

Childrens Chest Congestion Relief

Guaifenesin Oral Solution, USP
EXPECTORANT

Relieves Chest Congestion
Thins and Loosens Mucus

Alcohol-Free
For Ages 4 to 12

Grape Flavor

 4 FL OZ (118mL)

INDEPENDENTLY TESTED SATISFACTION GUARANTEED PV
DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING
   

*This product is not manufactured or distributed by Reckitt Benckiser Inc. distributor of Childrens Mucinex®

If for Any reason you are not satisfied with this product, please return it to the store where purchased for a full refund.

DISTRIBUTED BY
CHAIN DRUG CONSORTIUM
3301 NW BOCA RATON BLVD
SUITE 101, BOCA RATON, FL 33431

BX-011

AptaPharmaPV ChildCCRelief Label

CHILDRENS CHEST CONGESTION RELIEF 
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-157
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DEXTROSE (UNII: IY9XDZ35W2)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
MALTITOL (UNII: D65DG142WK)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPE (Grape Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-157-04118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34109/01/2012
Labeler - Chain Drug Consortium, LLC (101668460)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(68016-157)

Revised: 4/2013
Document Id: 3df087e5-2756-4337-b933-934c64ae48fe
Set id: c875ed06-3806-4ca7-843e-af5df10bf265
Version: 1
Effective Time: 20130401
 
Chain Drug Consortium, LLC