ALCOHOL PREP PAD- isopropyl alcohol swab

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Compre agora

Ingredientes ativos:

Isopropyl alcohol (UNII: ND2M416302) (Isopropyl alcohol - UNII:ND2M416302)

Disponível em:

Target Corporation

DCI (Denominação Comum Internacional):

Isopropyl alcohol

Composição:

Isopropyl alcohol 0.70 mL

Via de administração:

TOPICAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

Antiseptic

Status de autorização:

OTC monograph not final

Características técnicas

                                ALCOHOL PREP PAD - ISOPROPYL ALCOHOL SWAB
TARGET CORPORATION
_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._
----------
DRUG FACTS
ACTIVE INGREDIENT
Isopropyl Alcohol 70% v/v
PURPOSE
Antiseptic
USE
For preparation of the skin prior to an injection
WARNINGS
FOR EXTERNAL USE ONLY.
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
DO NOT USE
with electrocautery procedures
in the eyes
STOP USE
if irritation and redness develop. If condition persists for more than
72 hours, consult a doctor.
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
Wipe injection site vigorously and discard.
OTHER INFORMATION
Store at room temperature 15°- 30° C (59° - 86° F)
INACTIVE INGREDIENT
purified water
QUES TIONS ?
CALL 1-800-910-6874
PACKAGE INFORMATION
up and up
NDC 11673-600-10
ALCOHOL PREP PADS
70% isopropyl alcohol
Compare to BD®*
antiseptic for preparation of skin prior to injection
100 count
100 INDIVIDUALLY WRAPPED PADS
Distributed by Target Corporation
Minneapolis, MN 55403
Made in U.S.A.
© 2009 Target Brands, Inc.
All Rights Reserved
Shop Target.com
*This product is not manufactured or distributed by Becton Dickinson
and Company, owner of the
registered trademark BD®.
ALCOHOL PREP PAD
isopropyl alcohol swab
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:116 73-6 0 0
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ISO PRO PYL A LCO HO L (UNII: ND2M416 30 2) (Iso pro pyl alco ho l -
UNII:ND2M416 30 2)
Iso pro pyl alco ho l
0 .70 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WA TER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:116 73-6 0 0 -10
10 0 in 1 BOX
1
1 in 1 PACKET
Target Corporation
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUM
                                
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