MAJOR® Benzocaine 20% Spray

Manufacturer
MAJOR® PHARMACEUTICALS
Effective date
2024-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:59:07

Label at a glance#

ProductBenzocaine
Active ingredientBENZOCAINE
Label structure13 sections

Dosage and administration

do not exceed recommended dosage adults and children 2 years of age and older: 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

Storage and handling

store at 15-30 °C (59-86 °F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 20%

Purpose

OTC - PURPOSE SECTION

Oral Anesthetic

INDICATIONS & USAGE SECTION

Uses for the temporary relief of occasional minor irritation and pain associated with sore mouth and throat

Warnings

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

  • if foil pouch has been previously opened
  • for teething
  • in children under 2 years of age

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If more than used for pain is accidently swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) Immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not exceed recommended dosage

adults and children 2 years of age and older: 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

STORAGE AND HANDLING SECTION

  • store at 15-30 °C (59-86 °F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

cherry flavor, polyethylene glycol, sucralose

Questions or comments?

OTC - QUESTIONS SECTION

(855) 879-4368

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAJOR®

NDC 0904-7301-66

Benzocaine 20% Spray 

Unit Dose Non-Aerosol Spray 

20% Benzocaine Oral Anesthetic 

25 Unit Dose Non-Aerosol Sprays 

0.017 fl.oz. (0.5 mL)

MPDP Benzocaine CartonMPDP Benzocaine Carton

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAJOR®

NDC 0904-7301-65

Benzocaine 20% Spray

Unit Dose Non-Aerosol Spray

20% Benzocaine Oral Anesthetic

1 Unit Dose Non-Aerosol Spray

0.017 fl.oz. (0.5 mL)

MPDP Benzocaine pouchMPDP Benzocaine pouch

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-7301BENZOCAINE (TOPICAL ANESTHETIC) SPRAY [MAJOR® PHARMACEUTICALS]1Unmatched20240715_42b007fa-32c0-4130-ab39-002b79b84a6e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0904-73010904-7301-65, 0904-7301-86

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
54dede60-16e8-46e1-a44f-caa138b4289142b007fa-32c0-4130-ab39-002b79b84a6e2025-09-17WarningsExact identifier
spl set id: 42b007fa-32c0-4130-ab39-002b79b84a6e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.