HENRY SCHEIN POVIDONE-IODINE PREP PAD- povidone-iodine swab

国: アメリカ合衆国

言語: 英語

ソース: NLM (National Library of Medicine)

有効成分:

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

から入手可能:

Henry Schein, Inc.

投与経路:

TOPICAL

処方タイプ:

OTC DRUG

適応症:

Antiseptic For preparation of the skin prior to surgery

認証ステータス:

OTC monograph not final

製品の特徴

HENRY SCHEIN POVIDONE-IODINE PREP PAD- POVIDONE-IODINE SWAB
HENRY SCHEIN, INC.
----------
DRUG FACTS
ACTIVE INGREDIENT
Povidone Iodine USP 10%
PURPOSE
Antiseptic
USE
For preparation of the skin prior to surgery
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.
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 area. Apply to the operative site prior to surgery
OTHER INFORMATION
1 % titratable iodine. Store at ambient temperatures
INACTIVE INGREDIENTS
alkyl glucoside, citric acid, glycerin, hydroxyethyl cellulose,
nonoxynol-10, potassium
iodide, purified water, sodium hydroxide
PRINCIPAL DISPLAY PANEL - 0.5 ML ITEM LABEL
NDC 0404-0121-01
HENRY SCHEIN
REF 570-1543
POVIDONE-IODINE
PREP PAD
10% Povidone-Iodine
For Professional and Hospital Use
Not Made with Natural Rubber Latex
HENRY SCHEIN
SEAL OF EXCELLENCE
1/Pouch
HENRY SCHEIN POVIDONE-IODINE PREP PAD
povidone-iodine swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:0404-0121
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
®
®
Henry Schein, Inc.
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)
IODINE
1 g in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
NONOXYNOL-10 (UNII: K7O76887AP)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:0404-0121-
01
8000 in 1 CASE
10/22/2019
1
0.5 mL in 1 POUCH; Type 0: Not a Combination
Product
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
M003
10/22/201