POVIDONE IODINE SWABSTICKS 4 TRIPLE- povidone-iodine swab

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

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

Disponível em:

Amsino healthcare (USA) inc.

Via de administração:

TOPICAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

for antiseptic skin preparation

Status de autorização:

OTC monograph not final

Características técnicas

POVIDONE IODINE SWABSTICKS 4 TRIPLE- POVIDONE-IODINE SWAB
AMSINO HEALTHCARE (USA) INC.
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POVIDONE IODINE SWABSTICKS 4" TRIPLE
_DRUG FACTS_
_ACTIVE INGREDIENT_
Povidone-lodine USP10%
_PURPOSE_
Antiseptic
_USE_
for antiseptic skin preparation
_WARNINGS_
do not use if allergic to iodine
do not use in the eyes
_STOP USE AND ASK A DOCTOR IF_
redness,irritation,swelling or pain persists or increases
infection occurs
_KEEP OUT OF REACH OF CHILDREN._
In case of accidental ingestion,seek professional assistance or
consult a poison control
center immediately.
Avoid pooling beneath patient.
ASK A DOCTOR BEFORE USE IF
_injuries are_
FOR EXTERNAL USE ONLY.
deep or puncture wounds
serious burns
_DIRECTIONS_
apply locally as needed
_OTHER INFORMATION_
1% titratable iodine
For hospital or professional use only
Store at room temperature.
Avoid excessive heat.
Not made with natural rubber latex.
_INACTIVE INGREDIENTS:_
Citric Acid,Alkyl Glucoside,Hydroxyethyl Cellulose,Nonoxynol-
10,Glycerin,Sodium Hydroxide,Potassium lodide,Purified Water.
PACKAGE LABELING:
POVIDONE IODINE SWABSTICKS 4 TRIPLE
povidone-iodine swab
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:72838-0360
ROUTE OF ADMINISTRATION
TOPICAL
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)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
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:72838-
0360-1
3 in 1 POUCH
01/30/2022
1
2 g in 1 APPLICATOR; Type 4: Device
Coated/Impregnated/Otherwise Combined with Drug
MARKETING INFORMATION
Amsino healthcare (USA) inc.
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETIN