AFTER BITE WIPE INSECT STING RELIEF- benzocaine,alcohol swab

United States - English - NLM (National Library of Medicine)

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Active ingredient:
Benzocaine, 6%, SD alcohol, 60%
Available from:
Adventure Ready Brands
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
Topical Analgesic Antiseptic - temporarily relieves pain and itching due to minor stings and insect bites - to help reduce bacteria on the skin - over large areas of the body - in the eyes - on broken skin or deep puncture wounds condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.
Authorization status:
OTC monograph not final
Authorization number:
90107-3623-1, 90107-3623-2

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AFTER BITE WIPE INSECT STING RELIEF- benzocaine,alcohol swab

Adventure Ready Brands

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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After Bite Wipe Insect Sting Relief

Active Ingredients

Benzocaine, 6%

SD alcohol, 60%

Purpos e

Topical Analgesic

Antiseptic

Us e

temporarily relieves pain and itching due to minor stings and insect bites

to help reduce bacteria on the skin

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

over large areas of the body

in the eyes

on broken skin or deep puncture wounds

Stop use and ask a doctor if

condition worsens or if symptoms persist for more than 7 days or clear up and occur 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 year of age and older: apply to affected area not more than 3 to 4 times daily.

children under 2 years of age: consult a doctor

Other information

Store at room temperature

Inactive Ingredient

Purified water

AFTER BITE WIPE INSECT STING RELIEF

benzocaine,alcohol swab

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:9 0 10 7-36 23

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

BENZO CAINE (UNII: U3RSY48 JW5) (BENZOCAINE - UNII:U3RSY48 JW5)

BENZOCAINE

6 mg in 10 0 mg

ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)

ALCOHOL

6 0 mg in 10 0 mg

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

Packag ing

#

Item Code

Package Description

Marketing Start

Date

Marketing End Date

1

NDC:9 0 10 7-36 23-1

10 0 0 mg in 1 PACKAGE; Type 0 : No t a Co mbinatio n

Pro duc t

12/0 1/20 20

2

NDC:9 0 10 7-36 23-

10 0 in 1 BOX

12/0 1/20 20

Adventure Ready Brands

2

10 0 0 mg in 1 PACKET; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph no t final

pa rt333E

12/0 1/20 20

Labeler -

Adventure Ready Brands (064437304)

Revised: 12/2020

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