STING RELIEF SWAB- benzocaine swab

Drug Labeling and Warnings

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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

• 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

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

KEEP OUT OF REACH OF CHILDREN

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.

Packaging

INGREDIENTS AND APPEARANCE

STING RELIEF SWAB 
benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87251-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	0.006 g  in 0.6 mL
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	0.12 g  in 0.6 mL

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87251-010-01	6 mL in 1 CARTON; Type 0: Not a Combination Product	04/14/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/14/2026

Labeler - 4 Visions LLC (144898309)