LIMPIA PECHO- dextromethorphan hbr, guaifenesin liquid 
Llorens Pharmaceutical International Division, 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.

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In each teaspoonful, 5 mL

Dextromethorphan HBr - 10 mg

Guaifenesin - 100 mg

Purpose

Cough Suppressant

Expectorant

Uses

Warnings

Do not exceed recommended dosage

Do not use

Ask a doctor before use if you have 

Stop use and ask a dotor if

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

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

Directions

 Age Dose
 Adults and children over 12 years of age 10 mL (2 tsp) every 4 hours
 Children 6 to under 12 years of age 5 mL (1 tsp) every 4 hours
 Children under 6 Ask a doctor

Inactive ingredients artificial and natural flavor, citric acid, methol, methylparaben, propylened glycol, propylparaben, purified water, sodium citrate, and sucralose.

Questions or Comments? 1-866-595-5598

LipiaPecho

LIMPIA PECHO 
dextromethorphan hbr, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54859-011
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
MENTHOL (UNII: L7T10EIP3A)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
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:54859-011-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34105/01/2019
Labeler - Llorens Pharmaceutical International Division, Inc. (037342305)

Revised: 6/2019
Document Id: 822df434-72cd-496b-b046-44c459642806
Set id: cbaea3e4-4c4b-4ff9-ae6f-95b6a2d3faf3
Version: 1
Effective Time: 20190609
 
Llorens Pharmaceutical International Division, Inc.