FOAMING HAND SANITIZER- benzalkonium chloride gel

Pajjiż: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ingredjent attiv:

BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)

Disponibbli minn:

HY-VEE INC

INN (Isem Internazzjonali):

BENZALKONIUM CHLORIDE

Kompożizzjoni:

BENZALKONIUM CHLORIDE 0.1 mL in 100 mL

Rotta amministrattiva:

TOPICAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

ANTIMICROBIAL TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.

L-istatus ta 'awtorizzazzjoni:

OTC monograph not final

Karatteristiċi tal-prodott

FOAMING HAND SANITIZER - BENZALKONIUM CHLORIDE GEL
HY-VEE 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._
----------
DRUG FACTS
ACTIVE INGREDIENT
BENZALKONIUM CHLORIDE 0.1 PERCENT
PURPOSE
ANTIMICROBIAL
USES
TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE.
RECOMMENDED FOR REPEATED USE.
WARNINGS
FOR EXTERNAL USE ONLY.
WHEN USING THIS PRODUCT
AVOID CONTACT WITH EYES. IF PRODUCT GETS INTO EYES, RINSE THOROUGHLY
WITH
WATER.
STOP USING THIS PRODUCT AND ASK DOCTOR IF
IRRITATION OR RASH DEVELOPS AND LASTS.
KEEP OUT OF REACH OF CHILDREN
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON
CONTROL CENTER IMMEDIATELY.
DIRECTIONS
PUMP DESIRED AMOUNT ONTO HANDS AND RUB UNTIL YOUR SKIN IS DRY.
CHILDREN
UNDER THE AGE OF 6 SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.
INACTIVE INGREDIENTS
WATER, POLYSORBATE 20, ETHYLHEXYL METHOXYCINNAMATE, BUTYL
METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE, PPG-26-BUTETH-26, PEG-
40 HYDROGENATED CASTOR OIL, ALOE BARBADENSIS LEAF JUICE, FRAGRANCE,
TETRASODIUM EDTA, DMDM HYDANTOIN, SODIUM HYDROXIDE, BLUE 1 (CI 42090),
YELLOW 5 (CI 19140).
QUESTION OR COMMENTS
1-800-289-8343
FRONT AND BACK LABELS
FOAMING HAND SANITIZER
benzalkonium chloride gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:4250 7-240
ROUTE OF ADMINISTRATION
TOPICAL
HY-VEE INC
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
0 .1 mL
in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PO LYSO RBATE 2 0 (UNII: 7T1F30 V5YH)
O CTINO XATE (UNII: 4Y5P7MUD51)
AVO BENZO NE (UNII: G6 3QQF2NOX)
O CTISALATE (UNII: 4X49 Y0 59 6 W)
PO LYO XYL 4 0 HYDRO GENATED CASTO R O IL (UNII: 7YC6 8 6 GQ8 F)
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
GREEN TEA LEAF (UNII: W2ZU1RY8 B