MEDICAINE STING AND BITE- benzocaine swab

국가: 미국

언어: 영어

출처: NLM (National Library of Medicine)

지금 구매하세요

제품 특성 요약 제품 특성 요약 (SPC)
28-11-2022

유효 성분:

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

제공처:

Dynarex Corporation

관리 경로:

TOPICAL

처방전 유형:

OTC DRUG

치료 징후:

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

승인 상태:

unapproved drug other

제품 특성 요약

                                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
                                
                                전체 문서 읽기
                                
                            

이 제품과 관련된 검색 알림