Bactimicina Childrens Cough and Cold

Dosage form: liquid
Ingredients: CHLORPHENIRAMINE MALEATE 1mg in 5mL, DEXTROMETHORPHAN HYDROBROMIDE 7.5mg in 5mL
Labeler: DLC Laboratories, Inc.
NDC Code: 24286-1551

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.

Bactimicina Liquid Children's Cough and Cold

Active ingredients (in each 5 mL tsp)

Chlorpheniramine maleate, USP 1 mg

Dextromethorphan HBr, USP 7.5 mg

Purposes

Antihistamine

Cough suppressant

Uses
  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • sneezing
    • itchy, watery eyes
    • itching of the nose or throat

Warnings

Do not use

  • to sedate a child or to make a child sleepy
  • 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
  • trouble urinating due to an enlarged prostate gland
  • glaucoma
  • a cough that occurs with too much phlegm (mucus)
  • a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema

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

When using this product
  • do not use more than directed 
  • marked drowsiness may occur 
  • avoid alcoholic drinks 
  • alcohol, sedatives, and tranquilizers may increase drowsiness 
  • be careful when driving a motor vehicle or operating machinery          
  • excitability may occur, especially in children

Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. 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. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions
  • do not take more than 4 doses in any 24-hour period

 
Age (years)                                      Dose                    
Under 6                              do not use       
6 - 11                                 2 teaspoons every 6 hours       
12 and over                        4 teaspoons every 6 hours    

Other information
  • each teaspoon contains: sodium 1 mg
  • store at 15-30° (59-86°F) 
  • dosage cup provided

Inactive ingredients

citric acid, FD&C red no. 40, glycerin, natural strawberry flavor, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

LIQUID
BACTIMICINA
®

Chlorpheniramine Maleate /
Antihistamine

Dextromethorphan HBr /
Cough Suppressant

Children's
Cough
& Cold

Ages 6 & Over

  Relieves:
• COUGH: up to 8 hours
• SNEEZING
• RUNNY NOSE
• ITCHY, WATERY EYES

Alcohol Free
Long-Acting

Strawberry Flavor

4 FL OZ (118 mL)

BACTIMICINA CHILDRENS COUGH AND COLD 
chlorpheniramine maleate, dextromethorphan hydrobromide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1551
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORPHENIRAMINE MALEATE (CHLORPHENIRAMINE) CHLORPHENIRAMINE MALEATE1 mg  in 5 mL
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE7.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
FD&C RED NO. 40 
PROPYLENE GLYCOL 
WATER 
SODIUM BENZOATE 
SORBITOL 
SUCRALOSE 
GLYCERIN 
Product Characteristics
Colorred (Red) Score    
ShapeSize
FlavorSTRAWBERRY (Natural Strawberry flavor) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:24286-1551-41 BOTTLE in 1 BOX
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/23/2009
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIOperations
DLC Laboratories, Inc.093351930MANUFACTURE(24286-1551), LABEL(24286-1551)

Revised: 07/2013
 
DLC Laboratories, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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