Страна: Соединенные Штаты
Язык: английский
Источник: NLM (National Library of Medicine)
Benzalkonium Chloride 0.11%
Broadway Products LLC
TOPICAL
OTC DRUG
Antiseptic FDA Registered antiseptic for the care and cleaning of piercings.
OTC monograph not final
DR. PIERCING AFTERCARE- BENZALKONIUM CHLORIDE SWAB BROADWAY PRODUCTS LLC _Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may_ _be marketed if they comply with applicable regulations and policies. FDA has not_ _evaluated whether this product complies._ ---------- BROADWAY PRODUCTS (AS PLD) - DR. PIERCING - AFTERCARE SWAB (81926-001) ACTIVE INGREDIENTS Benzalkonium Chloride 0.11% PURPOSE Antiseptic USE FDA Registered antiseptic for the care and cleaning of piercings. WARNINGS: FOR EXTERNAL USE ONLY.If redness, irritation, infection or swelling occurs, discontinue use and consult a physician. Keep out of eyes. Do not insert into the ear canal. Store at room temprature. Keep out of reach of children. DIRECTIONS: 1. Hold swab with the colored round marker end up. 2. Bend the colored round marker tip until it "snaps". 3. Liquid flows down into the white tip. 4. Apply medicated tip to piercing. Dispose. OTHER INGREDIENTS Isotonic Saline Solution, Aloe Vera, Allantoin, Panthenol/Pro-Vitamin B5. DR. PIERCING AFTERCARE benzalkonium chloride swab PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:81926-001 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZ ALKONIUM CHLORIDE 1.1 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH Broadway Products LLC METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) PANTHENOL (UNII: WV9CM0O67Z) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) MAGNESIUM NITRATE (UNII: 77CBG3UN78) CUPRIC NITRATE (UNII: 9TC879S2ZV) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) TROLAMINE (UNII: 9O3K93S3TK) SODIUM CHLORIDE (UNII: 451W47IQ8X) ALLANTOIN (UNII: 344S277G0Z) ALOE VERA LEAF (UNII: ZY81Z83H0X) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:81926- 001-36 36 in 1 CASE 01/01/2021 1 0.15 mL in 1 APPLICATOR; Type 0: Not a Combinatio Прочитать полный документ