Nazione: Stati Uniti
Lingua: inglese
Fonte: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
CWGC LA Inc.
BENZALKONIUM CHLORIDE
BENZALKONIUM CHLORIDE 0.13 g in 100 mL
TOPICAL
OTC DRUG
- For hand washing to reduce bacteria on the skin. Recommended for repeat use. Stop use and ask doctor if irritation or redness develops and persists.
OTC monograph not final
SIERRA SOFT NON-ALCOHOL FOAM HAND SANITIZER- BENZALKONIUM CHLORIDE SOLUTION CWGC LA INC. _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._ ---------- CWGC (AS PLD) - SIERRA SOFT NON-ALCOHOL FOAM HAND SANITIZER (70415-106) ACTIVE INGREDIENT BENZALKONIUM CHLORIDE 0.13% PURPOSE Antibacterial USES For hand washing to reduce bacteria on the skin. Recommended for repeat use. _WARNINGS_ For external use only. Avoid contact with eyes - in case of contact, flush eyes with water. Keep out of reach of children. If swallowed, get immediate medical attention. Stop use and ask doctor if irritation or redness develops and persists. _DIRECTIONS_ Apply foam sanitizer to hands. Rub over surfaces of both hands for 15 seconds. No rinsing required. INACTIVE INGREDIENTS Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance. SIERRA SOFT NON-ALCOHOL FOAM HAND SANITIZER benzalkonium chloride solution PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:70415-106 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZ ALKONIUM CHLORIDE 0.13 g in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) COCO GLUCOSIDE (UNII: ICS790225B) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) CWGC LA Inc. ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:70415- 106-11 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2016 2 NDC:70415- 106-21 18925 mL in 1 PAIL; Type 0: Not a Combination Product 10/04/2017 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE OTC monograph not final part333E Leggi il documento completo