STING RELIEF PAD- benzocaine,isopropyl alcohol swab

Pajjiż: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ingredjent attiv:

BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5), ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)

Disponibbli minn:

Hubei Chenteng Healthcare Co.,Ltd.

INN (Isem Internazzjonali):

BENZOCAINE

Kompożizzjoni:

BENZOCAINE 60 mg

Rotta amministrattiva:

TOPICAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

Topicaln Anesthetic Antiseptic Prevent infection of minor scrapes and temporary relief of itching of insect bites

L-istatus ta 'awtorizzazzjoni:

OTC monograph not final

Karatteristiċi tal-prodott

STING RELIEF PAD- BENZOCAINE,ISOPROPYL ALCOHOL SWAB
HUBEI CHENTENG HEALTHCARE CO.,LTD.
_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._
----------
STING RELIEF PAD
ACTIVE INGREDIENT
Benzocaine, 6%
Isoprophyl Alcohol, 60.0%
PURPOS E
Topicaln Anesthetic
Antiseptic
US E
Prevent infection of minor scrapes and temporary relief of itching of
insect bites
FOR EXTERNAL USE ONLY
DO NOT USE in the eyes. If Contact Occurs, rinse thoroughly with
water.
STOP USE If irritation, redness or other symptoms develop.
CAUTION. If swallowed, get medical help or contact a poison control
center right away. Consult a doctor
if condition persists or gets worse.
DIRECTIONS
Apply to affected area 3 or 4 times daily. For adults and children 2
years of age and older.
Keep Out of Reach of Children
INACTIVE INGREDIENTS
Purified Water
PACKAGE LABEL:
STING RELIEF PAD
benzocaine,isopropyl alcohol swab
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:7150 9 -0 0 0
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 0 mg
ISO PRO PYL ALCO HO L (UNII: ND2M416 30 2) (ISOPROPYL ALCOHOL -
UNII:ND2M416 30 2)
ISOPROPYL ALCOHOL
6 0 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:7150 9 -
0 0 0 -0 0
1 in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System
(syringe, patch, etc.)
0 6 /21/20 17
0 4/30 /20 22
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MONOGRAPH CITATION
MARKE TING START DATE
MARKE TING END DATE
Hubei Chenteng Healthcare Co.,Ltd.
OTC mo no graph no t final
pa rt348
0 6 /21/20 17
0 4/30 /20 22
LABELER -
Hubei Chenteng Healthcare Co.,Ltd. (544504326)
Revised: 5/2019