BACTIMICINA CHILDRENS COUGH AND COLD- chlorpheniramine maleate, dextromethorphan hydrobromide liquid

Bactimicina Childrens Cough and Cold by

Drug Labeling and Warnings

Bactimicina Childrens Cough and Cold by is a Otc medication manufactured, distributed, or labeled by DLC Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active ingredients (in each 5 mL = 1 teaspoon)	Purposes
Chlorpheniramine maleate, USP 1 mg	Antihistamine
Dextromethorphan HBr, USP 7.5 mg	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
  • itchy, watery eyes
  • sneezing
  • 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 (10 mL) every 6 hours
12 and over	4 teaspoons (20 mL) every 6 hours

Other information

• each teaspoon (5 mL) contains: sodium 1 mg
• store at 15-30°C (59-86°F)
• dosage cup provided

Inactive ingredients

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

Questions

1-800-858-3889

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Manufactured by:
DLC Laboratories, Inc.
Paramount, CA 90723 USA

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)

INGREDIENTS AND APPEARANCE

BACTIMICINA CHILDRENS COUGH AND COLD 
chlorpheniramine maleate, dextromethorphan hydrobromide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24286-1551
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	1 mg  in 5 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	7.5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C RED NO. 40 (UNII: WZB9127XOA)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
GLYCERIN (UNII: PDC6A3C0OX)

Product Characteristics
Color	red (Red)	Score
Shape		Size
Flavor	STRAWBERRY (Natural Strawberry flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24286-1551-4	1 in 1 BOX	10/23/2009
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	10/23/2009

Labeler - DLC Laboratories, Inc. (093351930)

Establishment
Name	Address	ID/FEI	Business Operations
DLC Laboratories, Inc.		093351930	MANUFACTURE(24286-1551) , LABEL(24286-1551)