PANATUSS PED- chlophedianol hydrchloride, dexchlorpheniramine maleate, pseudoephedrine hydrochloride liquid 
Seyer Pharmatec, 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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Drug Facts

Active Ingredients                         Purpose
(in each 5 mL teaspoonful)

Chlophedianol HCl 25 mg ...................... Cough Suppressant

Dexchlorpheniramine Maleate 2 mg ......... Antihistamine

Pseudoephedrine HCl 60 mg ................... Nasal Decongestant

Purpose

Cough Suppressant

Antihistamine

Nasal Decongestant

Uses

Temporarily calms cough due to minor throat and bronchial irritation as may occur with the common cold

  • calms the cough control center and relieves coughing
  • non narcotic cough suppressant for the temporary relief of cough
  • temporarily relieves runny nose and alleviates sneezing, itching of the nose or throat and itchy, watery eyes due to hay fever or other upper respiratory allergies
  • temporarily relieves nasal congestion due to the common cold
  • helps decongest sinus openings and passages; temporarily relieves sinus congestion and pressure

Warnings

When using this product

  • use only as directed by physician
  • may cause excitability especially in children
  • may cause marked drowsiness; alcohol, sedatives and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages while taking this product
  • use caution when driving a motor vehicle or operating machinery


Do not use

  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product
  • if you have a breathing problem such as emphysema or chronic bronchitis, or if you have glaucoma or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor
  • if you are taking sedatives or tranquilizers, without first consulting your doctor
Stop use and ask a doctor if
  • nervousness, dizziness or sleeplessness occur
  • condition lasts for more than 7 days, comes back, or is accompanied by fever, rash or persistent headache. These could be signs of serious condition

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

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

Directions

  • take every 6 hours, not to exceed 4 doses in 24 hours or as directed by a physician

Adults and Children 12 years of age and older
1 teaspoonful (5 mL)
Children 6 to under 12 years of age
1/2 teaspoonful (2.5 mL)
Children under 6 years of age
Ask a doctor

Inactive ingredients

Citric acid, flavor, methylparaben, potassium citrate, potassium sorbate, propylparaben, propylene glycol, purified water, sorbitol, sucralose, xanthan gum

Questions or comments?1-888-782-3585

panatussped

PANATUSS PED 
chlophedianol hydrchloride, dexchlorpheniramine maleate, pseudoephedrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11026-2775
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y) (CHLOPHEDIANOL - UNII:42C50P12AP) CHLOPHEDIANOL HYDROCHLORIDE25 mg  in 5 mL
DEXCHLORPHENIRAMINE MALEATE (UNII: B10YD955QW) (DEXCHLORPHENIRAMINE - UNII:3Q9Q0B929N) DEXCHLORPHENIRAMINE MALEATE2 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE60 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorFRUIT (Tropical Fruit) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11026-2775-41 in 1 CARTON12/15/201201/30/2021
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34112/15/201201/30/2021
Labeler - Seyer Pharmatec, Inc. (832947126)

Revised: 10/2021
 
Seyer Pharmatec, Inc.