ALCOHOL PREP PAD- isopropyl alcohol swab

Country: Сједињене Америчке Државе

Језик: Енглески

Извор: NLM (National Library of Medicine)

Купи Сада

Активни састојак:

ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)

Доступно од:

Shandong Haiyan Medical Manufacture Co., Ltd.

INN (Међународно име):

ISOPROPYL ALCOHOL

Састав:

ISOPROPYL ALCOHOL 0.7 mL

Пут администрације:

TOPICAL

Тип рецептора:

OTC DRUG

Терапеутске индикације:

For preparation of skin prior to injection.

Статус ауторизације:

OTC monograph final

Карактеристике производа

                                ALCOHOL PREP PAD- ISOPROPYL ALCOHOL SWAB
SHANDONG HAIYAN MEDICAL MANUFACTURE 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._
----------
42339-001 ALCOHOL PREP PAD 70% ISOPROPYL ALCOHOL SHANDONG HAIYAN
MEDICAL MANUFACTURE CO., LTD. DRUG FACTS WWW. HAIYAN-MEDICAL.COM
ACTIVE INGREDIENT
Isopropyl Alcohol 70%v/v
PURPOSE
Antiseptic
USE
For preparation of skin prior to injection.
WARNINGS
For External use only.
Flammable,keep away from fire or flame.
Do not use with electrocautery procedures in eyes.
Stop use and ask a doctor if irritation and redness develop,condition
persists for more
than 72 hours .
KEEP OUT OF REACH OF CHILDREN
In case of accidental ingestion, seek professional assistance or
consult a PoisonControl
Center immediately.
DIRECTIONS
Wipe injection site vigorously and discard.
INACTIVE INGREDIENTS
purified water
section text here
ALCOHOL PREP PAD
isopropyl alcohol swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:42339-001
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL -
UNII:ND2M416302)
ISOPROPYL ALCOHOL
0.7 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:42339-
001-01
15 in 1 CONTAINER
12/01/2017
1
200 in 1 BOX; Type 0: Not a Combination Product
2
NDC:42339-
001-04
100 in 1 CONTAINER
12/01/2017
2
50 in 1 BOX; Type 0: Not a Combination Product
3
NDC:42339-
001-02
100 in 1 CONTAINER
12/01/2017
3
100 in 1 BOX; Type 0: Not a Combination Product
4
NDC:42339-
001-03
3000 in 1 CONTAINER; Type 0: Not a Combination
Product
12/01/2017
5
NDC:42339-
001-05
30 in 1 CASE
12/01/2017
5
36 in 1 BOX; Type 0: Not a Combination Product
6
NDC:42339-
001-06
24 in 1 CASE
12/01/2017
6
50 in 1 BOX; Type 0: 
                                
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