SANITECT ANTIBACTERIAL HAND- benzalkonium chloride soap soap

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

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

Available from:

Aquagenics Technologies

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

Antibacterial For handwashing , helps eliminate bacteria on hands. Stop use and ask a doctor if irritation or rash develops.

Authorization status:

OTC monograph not final

Summary of Product characteristics

SANITECT ANTIBACTERIAL HAND- BENZALKONIUM CHLORIDE SOAP SOAP
AQUAGENICS TECHNOLOGIES
_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._
----------
ACTIVE INGREDIENT(S)
Benzalkonium Chloride 0.13% Purpose: Antibacterial
PURPOSE
Antibacterial
USES
For handwashing , helps eliminate bacteria on hands.
WARNINGS
For external use only.
WHEN USING THIS PRODUCT
When using this product avoid contact with eyes. In case of contact,
rinse eyes
thoroughly with water.
Stop use and ask a doctor if irritation or rash develops.
Keep out of reach of children. In case of accidental ingestion, get
medical help or contact
a Poison Control Center immediately.
STOP USE AND ASK DOCTOR IF
Stop use and ask a doctor if irritation or rash develops.
Keep out of reach of children. In case of accidental ingestion, get
medical help or contact
a Poison Control Center immediately.
DIRECTIONS
Pump onto wet hands, vigorously work into a lather and rinse
thoroughly.
OTHER INFORMATION
Store in a cool dry place below 104F
INACTIVE INGREDIENTS
Water, lauramine Oxide, Cocamidopropyl Betaine, Coco Glucoside,
Glycerin, Lavender
Oil, Citric Acid, Methylchloroisothiazolinone.
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
NDC: 73763-466-01
SANITECT ANTIBACTERIAL HAND
benzalkonium chloride soap soap
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:73763-466
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
COCO GLUCOSIDE (UNII: ICS790225B)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
Aquagenics Technologies
LAVENDER OIL (UNII: ZBP1YXW0H8)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
GLYCERIN (UNII: P