ANCOS SILVER ION HAND SANITIZER gel

Ancos Silver Ion Hand Sanitizer by

Drug Labeling and Warnings

Ancos Silver Ion Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Anson Bio-Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Main Active Ingredients and Content

Silver ion: 0.01%, Ethyl alcohol: 62%(v/v)

Purpose

Antibacterial

Uses

The product has antibacterial effect on E coli, Staphylococcus aureus and Candida albicans, and can be used for hand disinfection in places such as intensive care unit, outpatient service, emergency room, ward and clinics, as well as in environment such as home and social places, especially when water is not available

Directions

Hand hygiene and disinfection: Take an appropriate amount of disinfectant to the palm, rub according to the hand disinfection code instructions, ensure that the sanitizer completely covers the skin of the hand sand wait for one minute until dry

Warning

• Sanitizer for external use, shall not betaken orally and shall be placed out of children's reach.
• Avoid using with antagonist drugs
• Those with allergies shall use

Other Tips

Protect from light and store airtight at room temperature

Precautions

Do not use this product in or near the eyes In case of contact, rinse eyes If irritation or rash appears and persists, stop using and consult the doctor.Please place out of children's reach. If swallowed, seek medical help or contact a Poison Control Center immediately

other ingredients

Purified water, Glycerol, Carbomer, Menthol

WHEN USING

STOP USE

KEEP OUT OF REACH OF CHILDREN

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ANCOS SILVER ION HAND SANITIZER 
ancos silver ion hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75139-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A)	SILVER CATION	0.01 g  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75139-006-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/28/2020

Labeler - Anson Bio-Technology Co., Ltd. (547087171)

Establishment
Name	Address	ID/FEI	Business Operations
Anson Bio-Technology Co., Ltd.		547087171	manufacture(75139-006)