Bactimicina Cough and Cold description, usages, side effects, indications, overdosage, supplying and lots more!

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Bactimicina Cough and Cold

DLC Laboratories, Inc.

Bactimicina Liquid Cough and Cold


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients (in each 5mL = 1 teaspoon)




Purposes




Bactimicina Cough and Cold Uses






Warnings

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 your prescription drug contains an MAOI, aska doctor of pharmacist before taking this product.

Ask a doctor before use if you have

heart disease

high blood pressure

thyroid disease

diabetes

trouble urinating due to an enlarged prostate gland

a cough that occurs with too much phlegm (mucus)



When using this product

do not use more than directed


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 6 doses in any 24-hour period






Other Information

each teaspoon contains: sodium 2mg

store 15-30C (59-86F)

dosage cup provided

Inactive Ingredients


Questions???

1-800-858-3889

www.bactimicina.com

Do not use if printed bottle wrap is broken or missing.

Manufactured by DE LA CRUZ PRODUCTS

a division of DLC Laboratories, Inc.

Paramount, CA 90723 USA

www.dlclabs.com (c)DLC

Liquid Bactimicina

Cough Suppressant/Expectorant/Nasal Decongestant

Cough and Cold

Relieves Coughs

Stuffy Nose









4fl oz (118 ml)

Bactimicina Cough and Cold

Bactimicina Cough and Cold

Bactimicina Cough and Cold

Bactimicina Cough and Cold

DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24286-1546
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 10 mg
Guaifenesin GUAIFENESIN 100 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
FD&C RED NO. 40
Strawberry
propylene glycol
water
saccharin sodium
SODIUM BENZOATE
sorbitol
GLYCERIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 118 in 1 BOTTLE
2 NDC:24286-1546-4 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-06-06


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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