WESTUSSIN DM NF- westussin dm nf liquid 
Westminster Pharmaceuticals, LLC

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WesTussin DM NF

Drug Facts

Active ingredients (in each 5 mL teaspoonful)Purpose
Dexbrompheniramine Maleate 2 mgAntihistamine
Dextromethorphan Hydrobromide 15 mgCough Suppressant
Phenylephrine Hydrochloride 7.5 mgNasal Decongestant

Uses

Uses temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:

Warnings

Do not exceed recommended dosage.

Do not use this product

  • 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.

Ask a doctor before use if you have

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
  • a cough that occurs with too much phlegm (mucus)
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

When using this product

  • excitability may occur, especially in children
  • may cause marked drowsiness
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • use caution when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache. A persistent cough may be a sign of a serious condition.
  • new symptoms occur

If pregnant or breastfeeding ask a health professional before use.

Keep out of reach of children.

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

Directions

Do not exceed recommended dosage

Adults and children 12 years of age and over:1 teaspoonful (5 mL) every 4 to 6 hours, not to exceed 6 teaspoonfuls in 24 hours
Children 6 to under 12 years of age:1/2 teaspoonful (2.5 mL) every 4 to 6 hours, not to exceed 3 teaspoonfuls in 24 hours
Children under 6 years of ageConsult a doctor.

Other information

Store at 59° - 86°F (15° - 30°C)

Inactive ingredients

Citric acid anhydrous, flavor, glycerin, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose, trisodium citrate dihydrate.

Questions?

Call weekdays from 9 AM to 5 PM EST at 1-844-221-7294. You may also report serious side effects to this phone number

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

NDC 69367-353-16

WesTussin DM NF

Antihistamine • Cough Suppressant
• Nasal Decongestant
SUGAR FREE / ALCOHOL FREE
DYE FREE / GLUTEN FREE

Each 5 mL (1 teaspoonful) contains:
Dexbrompheniramine Maleate
2 mg
Dextromethorphan HBr
15 mg
Phenylephrine HCl
7.5 mg

Strawberry Flavor

TAMPER EVIDENT: Tamper evident by foil seal under
cap. Do not use if foil seal is broken or missing.

16 OZ (473 mL)

Westminster
Pharmaceuticals

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
WESTUSSIN DM NF 
westussin dm nf liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69367-353
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE7.5 mg  in 5 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 5 mL
DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE2 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
Product Characteristics
Color    Score    
ShapeSize
FlavorSTRAWBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69367-353-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH DRUGM01207/19/2023
Labeler - Westminster Pharmaceuticals, LLC (079516651)

Revised: 7/2023
Document Id: 229e97f4-f9ac-4cd6-a3c0-a357d7f897a5
Set id: 4e0f9f97-a31c-41ac-9d6c-d81efd20fcef
Version: 2
Effective Time: 20230719
 
Westminster Pharmaceuticals, LLC