G-BUCAL-C- menthol, unspecified form and zinc chloride spray 
MCLAREN MEDICAL INC

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.

----------

G-BUCAL-C

DRUG FACTS

Active Ingredients (in each 30 mL)Purpose
Menthol 0.15%Anesthetic/Analgesic
Zinc Chloride 0.1%Astringent

INDICATIONS

For the temporary relief of occasional minor throat irritation, pain, sore mouth, sore throat, pain associated with canker sores, pain due to minor irritation or injury of the mouth and gums, pain due to minor dental procedures, pain due to minor irritations caused by dentures or orthodontic appliance, sore gums due to teething in infants and children 4 months of age and older.

DIRECTION FOR SPRAY

Spray G-Bucal-C several times as directed by physician or dentist to affected are in the mouth or lips. Children under 12 years of age should be supervised in the use of this product. Children under two years of age consult a doctor or dentist. As a gargle or mouthwash, ½ teaspoon in a half glass of warm water. Gargle swish around the mouth or allow to remain in place at least 1 minute and then spit out. Use up to 4 times daily or as directed by a dentist or doctor.

INACTIVE INGREDIENTS

Benzocaine, cetylpyridinium chloride, citric acid, glycerin, peppermint oil, polyethylene glycol, purified water, sodium citrate and sodium saccharin.

Each 30mL Contains:

Cetylpyridinium Chloride30 mg
Benzocaine600 mg
Menthol45 mg
Zinc Chloride30 mg

WARNINGS

If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. Do not use this product for more than 7 days unless directed by a dentist or doctor. If irritation, pain or redness persists or worsens, or if swelling, rash or fever develops, see your dentist or doctor promptly. DO NOT EXCEED RECOMMENDED DOSAGE. Do not use this product if you have history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. Discontinue use and consult a doctor if irritation persists or increases or a rash appears on the skin. Fever and nasal congestion are not symptoms of teething and may indicate the presence of infection. If these symptoms persist, consult your doctor. DO NOT USE IN OR NEAR THE EYES. In the event of accidental contact with eyes, flush immediately and continuously for ten minutes. See immediate medical attention if pain or irritation persists.

KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using this product.

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Label

NDC-43913-402-30

G-Bucal-C
Oral Solution Spray

Anesthetic • Astringent
Alcohol Free • Peppermint Flavor

1 FL OZ (30 mL)

For Dispensing Under
Pharmaceutical Supervision Only

McLaren Medical

Principal Display Panel - 30 mL Bottle Label
G-BUCAL-C 
menthol, unspecified form and zinc chloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43913-402
Route of AdministrationOROPHARYNGEAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM45 mg  in 30 mL
ZINC CHLORIDE (UNII: 86Q357L16B) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION30 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
BENZOCAINE (UNII: U3RSY48JW5)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
Product Characteristics
Color    Score    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43913-402-3030 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35601/01/2012
Labeler - MCLAREN MEDICAL INC (013770591)

Revised: 6/2015
Document Id: 8cf80886-2241-4e7c-af0e-50da491bf38e
Set id: 31690548-0a55-4d72-8733-591ba3a9be92
Version: 1
Effective Time: 20150629
 
MCLAREN MEDICAL INC