MEDICAINE STING AND BITE- benzocaine swab

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

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Active ingredient:
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)
Available from:
Dynarex Corporation
Administration route:
TOPICAL
Prescription type:
OTC DRUG
Therapeutic indications:
uses for temporary relief of pain and itching associated with insect bites and stings for temporary relief of pain and itching
Authorization status:
unapproved drug other
Authorization number:
67777-405-01

MEDICAINE STING AND BITE- benzocaine swab

Dynarex Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been

approved by FDA. For further information about unapproved drugs, click here.

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1407 Medicaine Insect Bite (Ampule) 67777-405-01

active ingredient each swab has benzocaine usp, l menthol

uses for temporary relief of pain and itching associated with insect bites and stings

keep out of reach of children. not for use with children less than 2 years old without medical advice. if

swallowed, get medical help immediately or contact a poison control center right away

revers cardboard sleeve then crush at dot between thumb and forefinger. once solution has saturated tip,

apply topically to the sting or bit. may be used on affected area(s) up to 4 times per day

store at room temperature away from light

purified water usp

for temporary relief of pain and itching

for external use only

medicaine sting and bit ampules latex free

MEDICAINE STING AND BITE

benzocaine swab

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 7777-40 5

Route of Administration

TOPICAL

Dynarex Corporation

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

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

BENZOCAINE

0 .12 g in 0 .6 mL

Inactive Ingredients

Ingredient Name

Stre ng th

MENTHO L (UNII: L7T10 EIP3A)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 7777-40 5-0 1

6 mL in 1 AMPULE; Type 0 : No t a Co mbinatio n Pro duct

0 2/14/19 76

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

unappro ved drug o ther

0 2/14/19 76

Labeler -

Dynarex Corporation (008124539)

Registrant -

Dynarex Corporation (008124529)

Revised: 3/2019

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