FIRST AID ONLY STING RELIEF PAD- benzocaine, isopropyl alcohol liquid

First Aid Only Sting Relief Pad by

Drug Labeling and Warnings

First Aid Only Sting Relief Pad by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Benzocaine 6.0%

Isopropyl Alcohol 60% w/v

Purpose

Topical Anesthetic

Antiseptic

INDICATIONS & USAGE

For the temporary relief of pain and itching associated with minor scrapes and insect bites.

First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only

Flammable, keep away from fire or flame

Do Not Use

• in eyes, if contact occurs flush with water ▪over large areas of the body

Consult a doctor ▪if condition worsens ▪if symptoms last for more than seven days or clear up and occur again ▪for deep puncture wounds

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control center right away.

Directions

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

▪Children under 2 years: consult physician

Inactive ingredient

Purified Water

SPL UNCLASSIFIED SECTION

Other information store at room temperature

PRINCIPAL DISPLAY PANEL

pouch label

INGREDIENTS AND APPEARANCE

FIRST AID ONLY STING RELIEF PAD 
benzocaine, isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-5204(NDC:59050-414)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	60 mg  in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	600 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-5204-05	100 in 1 BOX	02/25/2022
1		0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 0924-5204-04	50 in 1 BOX	02/25/2022
2		0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 0924-5204-03	25 in 1 BOX	02/25/2022
3		0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
4	NDC: 0924-5204-02	10 in 1 BOX	02/25/2022
4		0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
5	NDC: 0924-5204-01	0.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	02/25/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/25/2022

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-5204) , repack(0924-5204)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-5204) , repack(0924-5204)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		117825595	manufacture(0924-5204)