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Bio-B Kids

Dosage form: liquid
Ingredients: Dextromethorphan Hydrobromide 15mg in 5mL, CHLORPHENIRAMINE MALEATE 4mg in 5mL, Phenylephrine Hydrochloride 10mg in 5mL
Labeler: Advanced Generic Corporation
NDC Code: 45737-218

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.

Drug Facts

Active Ingredients: (in each 5 mL tsp.)              Purpose

Chlorpheniramine Maleate 4 mg................................Antihistamine

Dextromethorphan Hydrobromide 15 mg.................. Cough Suppressant

Phenylephrine HCl 10 mg.................................. Decongestant


  • temporarily relieves these symptoms due to cold, hay fever or other upper respiratory allergies
  • runny nose, sneezing, itching of the nose or throat, and itchy watery eyes
  • cough due to minor throat and bronchial irritation
  • nasal congestion


  • ask your doctor before use if you have
  • heart disease
  • diabetes
  • high blood pressure
  • thyroid disease
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • cough that occurs with too much phlegm (mucus)
  • chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema.
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers


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 you are taking a prescription drug that contains an MAOI;
ask your doctor or pharmacist before taking this product.

Stop Use and ask a doctor if
  • You get nervous, dizzy or sleepless
  • symptoms do not improve within 7 days, tend to recur or are accompanied by fever and rash or persistent headache. These may be symptoms of a serious condition.
When using this product
  • do not exceed recommended dosage
  • may cause excitability especially in children
  • may cause drowsiness, alcohol, sedatives, tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverage while taking this product
  • use caution when driving a motor vehicle or operating machinery

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

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

Directions Do not exceed 6 doses in 24 hours.

adults and children 12 years of age and over take 1 teaspoonful (5 mL) every 4 to 6 hours

children 6 to under 12 years of age take 1/2 teaspoonful (2.5 mL) every 4 to 6 hours

children under 6 years of age  consult a doctor

Other information  store at room temperature 15°- 30°C (59° - 86°F). Tamper evident by imprinted heat seal under cap. Do not use if there is evidence of tampering

Tamper Evident Feature:
Do not use if seal under cap (or cello-band over cap) is torn, broken or missing.

Questions or comments? 1-305-403-3788
Manufactured For: Advanced Generic Corporation, Miami, FL 33166.

Inactive ingredients Glycerin, propylene glycol, methylparaben, propylparaben, saccharin sodium, citric acid, sodium citrate, FD and C Red No. 40, strawberry flavor and purified water

dextromethorphan,chlorpheniramine maleate, phenylephrine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45737-218
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide15 mg  in 5 mL
Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride10 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
Citric Acid Monohydrate 
Propylene Glycol 
Sodium Citrate 
Saccharin Sodium 
FD&C RED NO. 40 
Product Characteristics
Color    Score    
FlavorSTRAWBERRY (Strawberry Flavor) Imprint Code
#Item CodePackage Description
1NDC:45737-218-16473 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/01/2009
Labeler - Advanced Generic Corporation (831762971)

Advanced Generic Corporation

Medically reviewed on Mar 28, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.