FIRST AID ONLY STING RELIEF PAD- benzocaine swab

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]

Active Ingredients

Benzocaine, 6% w/v

Isopropyl Alcohol 60% w/v

Purpose

Topical Anesthetic

Antiseptic

INDICATIONS & USAGE

Use

For the temporary relief of pait and itching associated with minor burns, scrapes and insect bites. First aid to help prevent infection in minor cuts, scrapes, and burns

DOSAGE & ADMINISTRATION

Directions

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

▪children under 2 years: consult a physician

WARNINGS

Warnings

For external use only

Flammable, keep away from fire or flames

Do not use

• In the eyes. If contact occurs, rinse thoroughly with water
• over large areas of the body

Stop use

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Keep out of reach of children.

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

INACTIVE INGREDIENT

Inactive Ingredients

Purified Water

STORAGE AND HANDLING

Other Information

Store at room temperature

Principal Display Panel - 0.4 mL Pouch Label

0.4 mL Pouch Label

INGREDIENTS AND APPEARANCE

FIRST AID ONLY STING RELIEF PAD 
benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-5203(NDC:65517-0005)
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	0.6 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-5203-01	0.4 mL in 1 POUCH; Type 0: Not a Combination Product	04/08/2019
2	NDC: 0924-5203-02	10 in 1 BOX	04/08/2019
2		0.4 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 0924-5203-03	25 in 1 BOX	04/08/2019
3	NDC: 0924-5203-01	0.4 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 0924-5203-04	100 in 1 BOX	04/08/2019
4	NDC: 0924-5203-01	0.4 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/08/2019

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-5203) , repack(0924-5203)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-5203) , repack(0924-5203)