BENZOCAINE- medicaine swab 
McKesson

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Medicaine Swabs

Active Ingredients (each swab)

Benzocaine USP (20%)

L‐Menthol USP (1%)

Purpose

Analgesic

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

Warnings

For external use only

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

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.

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 Information Store at room temperature away from light.

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.

Questions? Call 1-800-777-4908

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 boxdrug factscase

BENZOCAINE 
medicaine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-9560
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL1 mg  in 1 g
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68599-9560-10.21 g in 1 BOX; Type 0: Not a Combination Product01/16/202006/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/16/202006/01/2024
Labeler - McKesson (023904428)
Establishment
NameAddressID/FEIBusiness Operations
James Alexander Corp.040756421manufacture(68599-9560)

Revised: 9/2021
Document Id: cb090ad6-5331-3f20-e053-2995a90aa2a2
Set id: 9c449c74-5741-10d6-e053-2995a90aca75
Version: 3
Effective Time: 20210902
 
McKesson