BC SINUS CONGESTION AND PAIN- acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride powder 
Medtech Products Inc.

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BC Sinus Pain and Congestion

Drug Facts                              

Active ingredients (in each powder)

Acetaminophen 650 mg
Chlorpheniramine maleate 4mg
Phenylephrine hydrochloride 10mg

Purposes

Pain reliever/Fever reducer
Antihistamine
Nasal decongestant

Uses

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

Allergy Alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

If a skin reaction occurs, stop use and seek medical help right away.

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are now taking a prescription monoamine oxidase inhibitor (MOAI) (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

  • liver disease
  • high blood pressure
  • diabetes
  • thyroid disease
  • glaucoma
  • heart disease
  • a breathing problem such as emphysema or chronic bronchitis
  • trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are taking

  • the blood thinning drug warfarin
  • sedatives or tranquilizers

When using this product

  • do not exceed recommended dosage
  • drowsiness may occur
  • avoid alcoholic drinks
  • excitability may occur, especially in children
  • be careful when driving a motor vehicle or operating machinery
  • alcohol, sedatives and tranquilizers may increase the drowsiness effect

Stop use and ask a doctor if

  • pain or nasal congestion gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • you get nervous, dizzy, or sleepless
  • redness or swelling is present
  • new symptoms occur

These could be signs of a serious condition.

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children. 

Overdose warning: Taking more than the recommended dose can cause serious health problems. In the case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Other information

Store below 25°C (77°F)

Inactive ingredients

magnesium stearate, maltodextrin, silica

Questions?

1-866-255-5197 bcpowder.com

TAMPER EVIDENT: DO NOT USE IF PACKET IS DAMAGED OR OPEN.

PRINCIPAL DISPLAY PANEL

BC™  Sinus Pain & Congestion

Acetaminophen       Pain Reliever / Fever Reducer
Chlorpheniramine       Maleate Antihistamine
Phenylephrine HCl       Nasal Decongestant

12 Powders

PRINCIPAL DISPLAY PANEL

BC™  Sinus Pain & Congestion 

Acetaminophen  	Pain Reliever / Fever Reducer
Chlorpheniramine 	Maleate  Antihistamine
Phenylephrine HCl  	Nasal Decongestant

12 Powders

BC  SINUS CONGESTION AND PAIN
acetaminophen, chlorpheniramine maleate, phenylephrine hydrochloride powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-221
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE4 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63029-221-1212 in 1 CARTON; Type 0: Not a Combination Product03/01/2016
2NDC:63029-221-044 in 1 CARTRIDGE; Type 0: Not a Combination Product03/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01303/01/2016
Labeler - Medtech Products Inc. (122715688)

Revised: 10/2024
Document Id: ca199885-37c4-45b9-8bf9-b325df614baf
Set id: b0e5db7f-fc7a-45cd-8407-b9e8a47be8cb
Version: 2
Effective Time: 20241025
 
Medtech Products Inc.