Drug Labeling and Warnings

Drug Details [pdf]

UEC MEDICAL INSECT STING RELIEF- isopropyl alcohol, and benzocaine swab 
United Exchange Corp.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredients                                                    Purpose

Isopropyl Alcohol, 70% v/v.................................... Antiseptic

Benzocaine 6% v/v............................................... Topical analgesic

Use

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

Warnings

For external use only.

Flammable, keep away from fire or flame

Do not use

• over large areas of the body
• in the eyes
• or raw or blistered areas

Stop use and ask a doctor

• if condition worsens or persists for more than 7 days or clears up and occurs again within a few days.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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 og age, consult a doctor

Inactive ingredient purified water

Distributed by:

UEC Medical Co.

17211 Valley View Ave.

Cerritos, CA 90703 USA

www.uecmedical.com

Toll Free: 1 800 814 8028

UEC MEDICAL INSECT STING RELIEF 
isopropyl alcohol, and benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-349
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	0.06 mg
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mg

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-349-25	25 in 1 CARTON	04/25/2016	10/29/2019
1		1 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 65923-349-10	100 in 1 CARTON	04/25/2016	10/29/2019
2		1 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 not final	part348	04/25/2016	10/29/2019

Labeler - United Exchange Corp. (840130579)

Revised: 10/2019

Document Id: 9614ff9a-3b18-3b3c-e053-2a95a90a535a

34390-5

Set id: 49802ed4-db8d-4510-9b47-1980c77db11c

Version: 2

Effective Time: 20191029