Land: USA
Språk: engelsk
Kilde: NLM (National Library of Medicine)
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)
Cardinal Health 200, Inc
TOPICAL
OTC DRUG
- For preparation prior to surgery - Helps to reduce bacteria that can potentially cause skin infection
OTC monograph not final
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 Les hele dokumentet