Benzocaine

Manufacturer
McKesson | James Alexander Corp.
Effective date
2021-09-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:36:59

Label at a glance#

ProductBenzocaine
Active ingredientLEVOMENTHOL, BENZOCAINE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (each swab)

Benzocaine USP (20%)

L‐Menthol USP (1%)

OTC - PURPOSE SECTION

Purpose

Analgesic

INDICATIONS & USAGE SECTION

Uses
For temporary relief of pain and itching associated with insect bites and stings.

WARNINGS SECTION

Warnings

For external use only

  • do not use in the eyes
  • not for prolonged use
  • do not apply other medications to the same affected areas unless advised by a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if condition for this preparation is used persists, or if a rash, irritation or allergic reaction develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
Not for use with children less than 2 years old without medical advice.
If swallowed, get medical help immediately or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
Reverse cardboard sleeve then crush at dot between thumb and forefinger. Once solution has saturated tip,
apply topically to the sting or bite. May be used on affected area(s) up to 4 times per day

OTHER SAFETY INFORMATION

Other Information Store at room temperature away from light.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: D&C Green Dye #5, D&C Yellow Dye #10, FD&C Blue Dye #1, PEG 300 NF, Isopropyl Alcohol USP, Purified Water USP.

OTC - QUESTIONS SECTION

Questions? Call 1-800-777-4908

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 68599-9560-1

McKesson

Medicaine Swabs

Sting and Bite Relief

For temporary relief of pain and itching associated with insect bites and stings.

Net Contents

0.02 fl oz

(0.6 mL)

MFR# 15991

15591 box15591 boxdrug factsdrug factscasecase

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68599-956068599-9560-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
cb090ad6-5331-3f20-e053-2995a90aa2a29c449c74-5741-10d6-e053-2995a90aca752021-09-02WarningsExact identifier
spl id: cb090ad6-5331-3f20-e053-2995a90aa2a2
spl set id: 9c449c74-5741-10d6-e053-2995a90aca75

Reported adverse events (FAERS/openFDA)#

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