Sting Relief Wipes by ProStat First Aid LLC STING RELIEF WIPES swab

Sting Relief Wipes by

Drug Labeling and Warnings

Sting Relief Wipes by is a Otc medication manufactured, distributed, or labeled by ProStat First Aid LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benzocaine, 6% w/v

Purpose

Topical Analgesic

Active Ingredient

Isopropyl Alcohol, 60% w/v

Purpose

Antiseptic

Use(s)

For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations

Warnings

For External Use Only

Flammable. Keep away from fire or flame.

When using

Avoid contact with eyes; if this occurs, rinse thoroughtly with water

Do not use

With electrocautery procedures

Stop use if

Irritation and redness develop

Condition worsens or symptoms persist for more than 7 days, or clear up and occur again within a few day; discontinue use and consult a doctor

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

For adults and children 2 years of age and older, apply to affected area not more than 3-4 times daily.

For children under 2 years of age, consult a doctor before use.

Other information

Store at room temperature 15º-30ºC (59º-86ºF)

Avoid excessive heat

Inactive Ingredients

Water

Questions and Comments?

1-888-900-2920 Monday-Friday, 8AM-4PM PST

Label

INGREDIENTS AND APPEARANCE

STING RELIEF WIPES 
sting relief wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58228-2204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	60 mg  in 100 mL
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	6 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58228-2204-1	1000 in 1 CASE	01/08/2024
1		10 in 1 BOX
1		2 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/08/2024

Labeler - ProStat First Aid LLC (061263699)