Sore Throat Logenzes Sore Throat

The listing

NDC product code

17856-6255 (labeller 17856, product 6255)

Labeller

ATLANTIC BIOLOGICALS CORP.

Brand name

Sore Throat Logenzes Sore Throat

Generic name

Benzocaine and Menthol

Dosage form

Lozenge

Route

oral

Marketing category

OTC MONOGRAPH DRUG M013

Marketing start

28 December 2012

Listing expires

31 December 2026

Pharmacologic class

Standardized Chemical Allergen [EPC]

RxNorm concept

824574

Active ingredients

Strengths as listed in the FDA National Drug Code Directory, retrieved 4 September 2026. "Other listings" counts every other product on this site containing the same ingredient at any strength.

What the label claims

These are read from this product's own label, not assigned by us and not inferred from the ingredient.

Stated purposeOral anesthetic

Stated useSore throatSore mouth, gums and canker sores

Drug Facts, as filed

Quoted from the label FDA holds for this product. Long fields are truncated. The panel printed on the package you are holding is the one that governs.

Active ingredient

(in each lozenge) Purpose Benzocaine 15 mg Oral pain reliever Menthol 3.6 mg Oral pain reliever

Purpose

Active ingredients (in each lozenge) Purpose Benzocaine 15 mg Oral pain reliever Menthol 3.6 mg Oral pain reliever

Uses

temporary relief of occasional sore throat sore mouth minor mouth irritation pain associated with canker sores

Warnings

Allergy alert Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or any 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, nausea or vomiting consult a doctor promptly. Do not use in a child under 5 years of age. Stop use and ask a doctor or dentist if sore mouth symptoms do not improve in 7 days irritation, pain or redness persists or worsens swelling, rash or fever develops If pregnant or breast-feeding, ask a health professional before use. Keep this and all drugs out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not exceed recommended dosage.

Stop use and ask a doctor if

Stop use and ask a doctor or dentist if sore mouth symptoms do not improve in 7 days irritation, pain or redness persists or worsens swelling, rash or fever develops

If pregnant or breast-feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

Keep this and all drugs out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

adults and children 5 years or older: allow lozenge to dissolve slowly in the mouth; may be repeated every 2 hours as needed or as directed by a doctor or dentist. children under 5 years of age: ask a doctor

Inactive ingredients

Glucose syrup, N&A flavoring, propylene glycol, red #40, sucrose, and water. Soybean oil used as processing aid.

Storage

Other information tamper evident packaging: Do not use if outer box or blister is open or damaged. store at room temperature protect contents from moisture

Other information

Call 1-800-616-2471

Label version 2, effective 24 November 2025. Retrieved from the openFDA drug label API on 4 September 2026. Read the full label on DailyMed.

Packages

The package NDC adds a third segment to the product code, identifying the pack size. See how to read an NDC.

Identical on the active ingredient

10 other listings state exactly the same active ingredient at exactly the same strength in the same dosage form, across 10 different labellers. They are not necessarily the same product: inactive ingredients, flavour and pack size differ, and this site does not compare prices.

Sources for this page

• FDA National Drug Code Directory entry for 17856-6255
• DailyMed label, set id 71a80e13-bda3-40fb-b4e7-45e9985e707c
• How Lozenges builds these pages