SILVER ION ANTIBACTERIAL GEL gel

Silver Ion Antibacterial Gel by

Drug Labeling and Warnings

Silver Ion Antibacterial Gel 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 ions, 0.05%.

Glycerol, 5%.

Purpose

Antibacterial

Scope of Use

The product is suitable for antibacterial skin surface

Directions

After cleaning the skin surface, apply it directly to the skin surface for 5minandletitdry naturally without washing after use.

Warning

The product has antibacterial effect on staphylococcus aureus, escherichia coli and candida albicans.

Other Tips

Place away from light, seal and store at room temperature.

Precautions

See instructions for details

other ingredients

Carbomer, PEG 400, Sodium Hydroxide, Purified Water etc.

WHEN USING

See instructions for details

STOP USE

See instructions for details

KEEP OUT OF REACH OF CHILDREN

See instructions for details

Package Label - Principal Display Panel

75139-007-01 3G

75139-007-02 5G

75139-007-03 10G

75139-007-04 20

75139-007-05 30G

INGREDIENTS AND APPEARANCE

SILVER ION ANTIBACTERIAL GEL 
silver ion antibacterial gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75139-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	5 g  in 100 g
SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A)	SILVER CATION	0.05 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75139-007-02	5 g in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2020
2	NDC: 75139-007-01	3 g in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2020
3	NDC: 75139-007-05	30 g in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2020
4	NDC: 75139-007-04	20 g in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2020
5	NDC: 75139-007-03	10 g 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	part334	04/28/2020

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

Establishment
Name	Address	ID/FEI	Business Operations
Anson Bio-Technology Co.,Ltd.		547087171	manufacture(75139-007)