MEDICAINE STING AND BITE- benzocaine swab

Země: Spojené státy

Jazyk: angličtina

Zdroj: NLM (National Library of Medicine)

Aktivní složka:

BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)

Dostupné s:

Dynarex Corporation

Podání:

TOPICAL

Druh předpisu:

OTC DRUG

Terapeutické indikace:

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

Stav Autorizace:

unapproved drug other

Charakteristika produktu

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._
----------
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
Dynarex Corporation
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:67777-405
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)
BENZ OCAINE
0.12 g in 0.6 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
MENTHOL (UNII: L7T10EIP3A)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:67777-405-
02
10 in 1 BOX
02/14/1976
1
NDC:67777-405-
01
6 mL in 1 AMPULE; Type 0: Not a Combination
Product
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
unapproved drug
other
02/14/1976
LABELER -
Dynarex Corporation (008124539)
REGISTRANT -
Dynarex Corporation (008124529)
Revised: 11/2022