البلد: الولايات المتحدة
اللغة: الإنجليزية
المصدر: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Dukal LLC
TOPICAL
OTC DRUG
First Aid Antiseptic Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds. In the eyes or apply over large areas of the body. If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.
OTC monograph not final
BZK TOWELETTE- BENZALKONIUM CHLORIDE SWAB DUKAL LLC ---------- 855 - BZK _DRUG FACTS_ ACTIVE INGREDIENTS Benzalkonium Chloride, 0.133% w/v PURPOSE First Aid Antiseptic USE Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds. DO NOT USE In the eyes or apply over large areas of the body. STOP USE If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse. CAUTION KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. DIRECTIONS Tear open packet, unfold and use as a washcloth. INACTIVE INGREDIENTS Sodium Bicarbonate, Water PRINCIPAL DISPLAY PANEL - 1.4 ML POUCH LABEL DUKAL CORPORATION REF 855 _NDC 65517-0004-1_ _BZK ANTISEPTIC_ _TOWELETTE_ Contains Benzalkonium Chloride 1/POUCH LATE MANUFACTURED FOR: DUKAL CORPORATION Ronkonkoma, NY 11779 www.dukal.com Questions? 1-800-243-0741 Made in China D07110604 Rev7 PRINCIPAL DISPLAY PANEL - 2.1 ML POUCH LABEL DUKAL™ CORPORATION REF 855C _NDC 65517-0004-2_ _NON-STERILE_ _BZK TOWELETTE_ Contains Benzalkonium Chloride For External Use Only 1/POUCH DUKAL CORPORATION (631) 656-3800 Ronkonkoma, NY 11779 www.dukal.com Made in China BZK TOWELETTE benzalkonium chloride swab PRODUCT INFORMATION Dukal LLC PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:65517-0004 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZ ALKONIUM CHLORIDE 1.33 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:65517- 0004-1 1.4 mL in 1 POUCH; Type 0: Not a Combination Product 01/01/2006 2 NDC:65517- 0004-2 2.1 mL in 1 POUCH; Type 0: Not a Combination Product 01/01/2006 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC Monograph Drug M003 01/01/ اقرأ الوثيقة كاملة