POVIDONE-IODINE PREP STERILE- povidone-iodine swab

Ülke: ABD

Dil: İngilizce

Kaynak: NLM (National Library of Medicine)

Aktif bileşen:

POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)

Mevcut itibaren:

Cardinal Health 200, Inc

Uygulama yolu:

TOPICAL

Reçete türü:

OTC DRUG

Terapötik endikasyonlar:

- For preparation prior to surgery - Helps to reduce bacteria that can potentially cause skin infection

Yetkilendirme durumu:

OTC monograph not final

Ürün özellikleri

POVIDONE-IODINE PREP STERILE- POVIDONE-IODINE SWAB
CARDINAL HEALTH 200, INC
----------
POVIDONE-IODINE PREP SWABSTICKS STERILE
DRUG FACTS
ACTIVE INGREDIENT
Povidone-Iodine USP 10%
PURPOSE
Antiseptic
USE
For preparation prior to surgery
Helps to reduce bacteria that can potentially cause skin infection
WARNINGS
FOR EXTERNAL USE ONLY.DO NOT APPLY TO PERSONS ALLERGIC TO IODINE
DO NOT USE
in the eyes.
ASK A DOCTOR BEFORE USE IF INJURIES ARE
deep wounds
puncture wounds
serious burns
STOP USE AND ASK A DOCTOR IF
irritation and redness develop
condition persists for more than 72 hours
infection occurs
AVOID POOLING BENEATH THE PATIENT.
Prolonged exposure to wet solution may cause skin irritation.
KEEP OUT OF REACH OF CHILDREN.
If swallowed or gets in eyes, get medical help or contact a Poison
Control Center right
away.
DIRECTIONS
Clean the area. Apply product to the operative site prior to surgery
using spong sticks
to prep desired area.
OTHER INFORMATION
1% titratable iodine
latex free
for hospital or professional use only
INACTIVE INGREDIENTS
Citric Acid, Alkyl Glucoside, Hydroxyethyl Cellulose, Nonoxynol-10,
Glycerin, Sodium
Hydroxide, Potassium Iodide, Purified Water
PRODUCT LABEL
POVIDONE-IODINE PREP STERILE
povidone-iodine swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:63517-251
ROUTE OF ADMINISTRATION
TOPICAL
Cardinal Health 200, Inc
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)
IODINE
100 mg in 1 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
NONOXYNOL-10 (UNII: K7O76887AP)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
WATER (UNII: 059QF0KO0R)
PACKAGING
#
ITEM
CODE
PACKAGE DESCRIPTION
MARKETING
START DATE
MARKETING
END DATE
1
NDC:63517-
251-21
50 in 1 BOX
04/29/2015
1
1 in 1 POUCH
1
2 g in 1 PATCH; Type 4: Device
Coated/Impregnated/Otherwise Combined with Drug
MARKETING INFORMATION
MARKETING
CATEGO