Kraj: Stany Zjednoczone
Język: angielski
Źródło: NLM (National Library of Medicine)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)
Mangiacotti, Inc
TOPICAL
OTC DRUG
- For hand sanitizing to decrease bacteria on the skin - Recommended for repeated use
OTC monograph not final
LAVENDER HAND SANITIZER- BENZALKONIUM CHLORIDE SPRAY MANGIACOTTI, 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._ ---------- LAVENDER HAND SANITIZER SPRAY _DRUG FACTS_ _ACTIVE INGREDIENT_ Benzalkonium Chloride 0.1% _PURPOSE_ Antimicrobial _USES_ For hand sanitizing to decrease bacteria on the skin Recommended for repeated use _WARNINGS_ FOR EXTERNAL USE ONLY WHEN USING THIS PRODUCT avoid contact with eyes. In case of eye contact, flush eyes with water. STOP USE AND ASK A DOCTOR IF irritation or redness develops, or if condition persists for more than 72 hours. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away. _DIRECTIONS_ Spray a small amount into palm of hands Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry _INACTIVE INGREDIENTS_ Water, cetrimonium chloride, lautrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, citric acid, fragrance with essential oils PACKAGE LABELING: LAVENDER HAND SANITIZER benzalkonium chloride spray PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:42926-007 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 mg in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) GLYCERETH-17 COCOATE (UNII: 3057VPT0KC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:42926-007- 01 1 in 1 TUBE 12/21/2020 01/31/2023 1 9 mL in 1 BOTTLE; Type 0: Not a Combination Product MARKETING INFORMATION MARKETING CATEGORY APPLICATION NU Przeczytaj cały dokument