EQUATE ANTIBACTERIAL FOAMING HAND SPRING SHOWERS- benzalkonium chloride liquid

Country: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ingredjent attiv:

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

Disponibbli minn:

Wal-Mart Stores Inc

INN (Isem Internazzjonali):

BENZALKONIUM CHLORIDE

Kompożizzjoni:

BENZALKONIUM CHLORIDE 1.3 mg in 1 mL

Rotta amministrattiva:

TOPICAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

- helps eliminate bacteria on the skin.

L-istatus ta 'awtorizzazzjoni:

OTC monograph not final

Karatteristiċi tal-prodott

EQUATE ANTIBACTERIAL FOAMING HAND SPRING SHOWERS- BENZALKONIUM
CHLORIDE LIQUID
WAL-MART STORES 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 0.13%
PURPOS E
Antibacterial
US ES
helps eliminate bacteria on the skin.
WARNINGS
For external use only.
WHEN USING THIS PRODUCT
avoid contact with eyes. If contact occurs, rinse eyes thoroughly with
water.
Stop using this product and ask doctor
if irritation and redness 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
Apply onto dry hands, work into a lather and rinse thoroughly.
OTHER INFORMATION
store at room temperature.
INACTIVE INGREDIENTS
Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance
(Parfum), Glycerin, Decyl
Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice,
Camellia Sinensis Leaf Extract,
Propylene Glycol, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate,
Citric Acid, Benzophenone-
4, Methylchloroisothiazolinone, Methylisothiazolinione, Blue 1 (CI
42090), Ext. Violet 2 (CI 60730).
LABEL COPY
EQUATE ANTIBACTERIAL FOAMING HAND SPRING SHOWERS
benzalkonium chloride liquid
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:49 0 35-0 14
ROUTE OF ADMINISTRATION
TOPICAL
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
1.3 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
CO CAMIDO PRO PYL BETAINE (UNII: 5OCF3O11KX)
PO LYSO RBATE 2 0 (UNII: 7T1F30 V5YH)
GLYCERIN (UNII: PDC6 A3C0 OX)
DECYL GLUCO SIDE (UNII: Z17H9 7EA6 Y)
HYDRO XYETHYL CELLULO SE ( 50 0 0 CPS AT 1%) (UNII: X70 SE6 2ZAR)
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
G