HURRICAINE TOPICAL ANESTHETIC LIQUID- benzocaine liquid

HurriCaine by

Drug Labeling and Warnings

HurriCaine by is a Otc medication manufactured, distributed, or labeled by Beutlich Pharmaceuticals, LLC, Dental Technologies Inc., Speciality Pharma Manufacturing, SWABPLUS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzocaine 20%

Purpose

Oral Anesthetic

Uses

for temporary relief of occasional minor irritation and pain associated with:

• canker sores
• sore mouth and throat
• minor injury of the mouth and gums
• minor dental procedures
• minor irritation of the mouth and gums caused by dentures or orthodontic appliances
  

Warnings

Methemoglobinemia warning:Use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops:
pale, gray, or blue colored skin (cyanosis)
headache
rapid heart rate
shortness of breath
dizziness or lightheadedness
fatigue or lack of energy

Allergy alert: Do not use if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics.

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, or irritation, pain, or redness persists or worsens, see your dentist or doctor promptly.

Do not use

Do not use

• if imprinted seal under cap is broken or missing
• for teething
• in children under 2 years of age

When using this product

When using this product avoid contact with eyes

Keep out of reach of children

Keep out of reach of children If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Directions

• do not exceed recommended dosage

adults and children 2 years of age and older: apply to the affected area. 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.

children under 12 years of age: should be supervised in the use of the product

children under 2 years of age: do not use

Other information

• store at 20°-25°C (68°-77°F)

Inactive ingredients

flavor, polyethylene glycol, sodium saccharin

Questions or comments?

1-800-238-8542

M-F: 8:00 a.m.- 4:30 p.m. ET

Principal Display Panel

NDC: 0283-0569-31

HURRICAINE®

Topical Anesthetic LIQUID

20% Benzocaine Oral Anesthetic

ORIGINAL WILD CHERRY

Manufactured for:

Beutlich® Pharmaceuticals, LLC

Bunnell, FL 32110

Made in the USA

1 fl. oz. 

PRINCIPAL DISPLAY PANEL

NDC: 0283-0569-72

PRINCIPAL DISPLAY PANEL

NDC: 0283-0569-02 

INGREDIENTS AND APPEARANCE

HURRICAINE  TOPICAL ANESTHETIC LIQUID
benzocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0283-0569
Route of Administration	DENTAL, PERIODONTAL, ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	200 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0283-0569-31	29.6 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/15/1969
2	NDC: 0283-0569-17	1 g in 1 PACKET; Type 0: Not a Combination Product	01/28/2020
3	NDC: 0283-0569-72	72 g in 1 APPLICATOR; Type 0: Not a Combination Product	05/15/1969
4	NDC: 0283-0569-02	2 g in 1 APPLICATOR; Type 0: Not a Combination Product	05/15/1969

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	05/15/1969

Labeler - Beutlich Pharmaceuticals, LLC (005209325)

Registrant - Beutlich Pharmaceuticals, LLC (005209325)

Establishment
Name	Address	ID/FEI	Business Operations
Dental Technologies Inc.		148312838	manufacture(0283-0569)

Establishment
Name	Address	ID/FEI	Business Operations
Speciality Pharma Manufacturing		013957125	manufacture(0283-0569)

Establishment
Name	Address	ID/FEI	Business Operations
SWABPLUS		116984439	manufacture(0283-0569)