BABINGTONSOAPCO- hand sanitizer gel gel

Quốc gia: Hoa Kỳ

Ngôn ngữ: Tiếng Anh

Nguồn: NLM (National Library of Medicine)

Thành phần hoạt chất:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Sẵn có từ:

Babington Soap Co Limited

Tuyến hành chính:

TOPICAL

Loại thuốc theo toa:

OTC DRUG

Chỉ dẫn điều trị:

Antiseptic, Hand Sanitizer Hand Sanitizer to help reduce bacteria on the skin. Stop use and ask a doctor if irritation and redness develop.

Tình trạng ủy quyền:

OTC monograph not final

Đặc tính sản phẩm

BABINGTONSOAPCO- HAND SANITIZER GEL GEL
BABINGTON SOAP CO LIMITED
_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._
----------
BABINGTON SOAP CO. 55ML
ACTIVE INGREDIENT(S)
Alcohol 66% v/v. Purpose: Antiseptic
PURPOS E
Antiseptic, Hand Sanitizer
US E
Hand Sanitizer to help reduce bacteria on the skin.
WARNINGS
Flammable. Keep away from fire or flame
For external use only.
When using this product keep out of eyes, ears, and mouth. In case of
contact with eyes, rinse eyes
thoroughly with water.
Stop use and ask a doctor if irritation and redness develop.
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center right
away.
Stop use and ask a doctor if irritation and redness develop.
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center right
away.
DIRECTIONS
Dispense onto dry hands and rub together thoroughly and then allow
product to dry without rinsing.
Do not use on open skin or wounds.
Not for use by children under 6 years old.
OTHER INFORMATION
Do not store above 106F.
If skin irritation or rash occurs discontinue use immediately.
May discolor some fabrics.
INACTIVE INGREDIENTS
Aqua, Polyquaternium 10, Chitosan, lactic acid organic, lemongrass
oil.
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
55 mL NDC: 80104-111-11
BABINGTONSOAPCO
hand sanitizer gel gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:8 0 10 4-111
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
6 6 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
PO LYQ UATERNIUM-10 ( 2 0 0 0 0 MPA.S AT 2 %) (UNII: N2GK4S7X4T)
CYMBO PO GO N SCHO ENANTHUS O IL (UNII: XE7K56 8 ILO)
WATER (UNII: 0 59 QF0 KO0 R)
LACTIC ACID (UNII: 33X0 4XA5AT)
CHITO SAN MEDIUM MO