Chloraseptic Sore Throat Liquid Center description, usages, side effects, indications, overdosage, supplying and lots more!

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Chloraseptic Sore Throat Liquid Center

Prestige Brands Holdings, Inc.

Chloraseptic Green Tea Lozenges




FULL PRESCRIBING INFORMATION

Drug Facts

(in each lozenge)

Benzocaine 6 mg

Oral Anesthetic/Analgesic

(in each lozenge)

Menthol 10 mg

Oral Anesthetic/Analgesic

Temporarily relieves:

  • occasional minor irritation, pain, sore throat and sore mouth

Allergy Alert: Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other “caine” anesthetics.

Sore Throat Warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 6 years of age unless directed by a doctor.

do not exceed recommended dosage.

  • sore mouth symptoms do not improve in 7 days
  • irritation, pain or redness persists or worsens
  • swelling, rash or fever develops

ask a health care professional before use.

In case of overdose or accidental poisoning, get medical help or contact a Poison Control Center right away.

  • Adults and children 6 years of age and over: Take 1 lozenge every 2 hours as needed. Allow lozenges to dissolve slowly in the mouth.
  • Children under 6 years of age: Consult a doctor or dentist.
  • Store between 59ºF and 86ºF (15ºC - 30ºC).
  • Protect from moisture.
  • Check expiration date before using.
  • Tamper Evident: Do not use if blister package with “Chloraseptic®” name has been disturbed or opened.

Corn Syrup, Epigallocatechin Gallate (ECGC), FD&C Blue #1, FD&C Yellow #5, Flavor, Honey, Propylene Glycol, Soy Lecithin, Sucrose, Water

1-800-552-7932 or www.chloraseptic.com

Chloraseptic® 
SORE THROAT
18 lozenges | Green Tea with real honey

Chloraseptic Sore Throat Liquid Center

Chloraseptic Sore Throat Liquid Center

Menthol and Benzocaine LOZENGE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67172-014
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 10 mg
BENZOCAINE Benzocaine 6 mg

Inactive Ingredients

Ingredient Name Strength
CORN SYRUP
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
GLYCERIN
LECITHIN, SOYBEAN
Sucralose
water
HONEY
propylene glycol

Product Characteristics

Color Size Imprint Code Shape
GREEN 4 mm C OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 18 in 1 BLISTER PACK
2 NDC:67172-014-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2010-08-01


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