BC DAYTIME MULTI-SYMPTOM- acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride powder 
Medtech Products 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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BC Daytime Multi-Symptom

Drug Facts                              

Active ingredients

(in each powder)                        
Acetaminophen 650 mg 
Dextromethorphan HBr 20mg
Phenylephrine hydrochloride 10mg

Purposes

Pain reliever/Fever reducer
Cough suppressant
Nasal decongestant

Uses

Warnings

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

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied by or followed by fever, headache, rash, nausea, or vomiting consult a doctor promptly.

Allergy Alert: Acetaminophen may cause severe skin reactions. Symptoms may include: ▪ skin reddening ▪ blisters ▪ rash. 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
  • heart disease
  • cough that occurs with too much phlegm (mucus)
  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use

if you are taking the blood thinning drug warfarin

When using this product,

do not use more than directed

Stop use and ask a doctor if

  • pain ,nasal congestion or cough 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
  • cough comes back or occurs with rash or headache that lasts.

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

Inactive ingredients

magnesium stearate, maltodextrin, silica

Questions?

1-866-255-5197 bcpowder.com

©2018 Distributed by Medtech Products Inc.
Tarrytown, New York 10591
A Prestige Brands Company
Made in USA

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

PRINCIPAL DISPLAY PANEL

BC™ Daytime Multi-Symptom

Acetaminophen – Pain Reliever / Fever Reducer
Dextromethorphan HBr – Cough Suppressant
Phenylephrine HCl – Nasal Decongestant

12 Powders

BC™ Daytime Multi-Symptom

Acetaminophen – Pain Reliever / Fever Reducer
Dextromethorphan HBr – Cough Suppressant
Phenylephrine HCl – Nasal Decongestant

12 Powders

PRINCIPAL DISPLAY PANEL

BC™ Daytime Multi-Symptom

Acetaminophen – Pain Reliever / Fever Reducer
Dextromethorphan HBr – Cough Suppressant
Phenylephrine HCl – Nasal Decongestant

4 Powders

BC™ Daytime Multi-Symptom

Acetaminophen – Pain Reliever / Fever Reducer
Dextromethorphan HBr – Cough Suppressant
Phenylephrine HCl – Nasal Decongestant

4 Powders

BC  DAYTIME MULTI-SYMPTOM
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63029-215
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 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:63029-215-044 in 1 CARTON; Type 0: Not a Combination Product05/07/2018
2NDC:63029-215-1212 in 1 CARTON; Type 0: Not a Combination Product05/07/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34105/07/2018
Labeler - Medtech Products Inc. (122715688)

Revised: 5/2018
Document Id: f7e5b2ad-68d8-45a6-8ee0-c8c29e590f57
Set id: 1f653f79-63b9-4c2b-8fe6-d7bb29d84636
Version: 3
Effective Time: 20180510
 
Medtech Products Inc.