FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Dongguan Mingyi Medical Products Co., Ltd.
Effective date
2020-09-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:14:50

Label at a glance#

ProductHAND SANITIZER
Active ingredientSILVER CATION
Label structure11 sections

Indications and uses

Uses Hand sanitizer to help reduce bacteria on skin.

Dosage and administration

place enough in your palm to thoroughly spread on both and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

store below 105.8°F.(41°C) may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Silver Ion 0.2%

​Purpose

OTC - PURPOSE SECTION

Antimicrobial

​Uses

INDICATIONS & USAGE SECTION

Uses Hand sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

This product is a hand sanitizer for external use.

Please do not eat it .Not suitable for children to play everywhere,keep out of reach of children. Store in a cool, dry place, away from light, sealed, moisture-proof.
Do not use in the eyes. Can be, used for wound disinfection, without any stimulation.

OTC - DO NOT USE SECTION

Do not use in the eyes. Can be, used for wound disinfection, without any stimulation.

OTC - WHEN USING SECTION

Please do not eat it .Not suitable for children to play everywhere,keep out of reach of children. Store in a cool, dry place, away from light, sealed, moisture-proof.
Do not use in the eyes. Can be, used for wound disinfection, without any stimulation.

OTC - STOP USE SECTION

/

Directions

DOSAGE & ADMINISTRATION SECTION

place enough in your palm to thoroughly spread on both and rub into the skin until dry.

Children under 6 years of age should be supervised when using this product.

Other Information

STORAGE AND HANDLING SECTION

store below 105.8°F.(41°C)
may discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Carbo-mer, Glycerin, Hydrogen peroxide, Essence

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74046-002-01 3ml74046-002-01 3ml74046-002-02 10ml74046-002-02 10ml74046-002-15 236ml74046-002-15 236ml74046-002-13 100ml74046-002-13 100ml74046-002-06 38ml74046-002-06 38ml74046-002-08 45ml74046-002-08 45ml74046-002-12 80ml74046-002-12 80ml74046-002-10 60ml74046-002-10 60ml74046-002-18 300ml74046-002-18 300ml74046-002-16 240ml74046-002-16 240ml74046-002-20 500ml74046-002-20 500ml74046-002-04 20ml74046-002-04 20ml74046-002-05 30ml74046-002-05 30ml74046-002-19 450ml74046-002-19 450ml74046-002-07 40ml74046-002-07 40ml74046-002-03 15ml74046-002-03 15ml74046-002-17 250ml74046-002-17 250ml74046-002-11 70ml74046-002-11 70ml74046-002-09 50ml74046-002-09 50ml74046-002-14 120ml74046-002-14 120ml

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74046-00274046-002-10, 74046-002-03, 74046-002-04, 74046-002-02, 74046-002-05, 74046-002-06, 74046-002-08, 74046-002-09, 74046-002-01, 74046-002-07, 74046-002-15, 74046-002-16, 74046-002-18, 74046-002-11, 74046-002-12, 74046-002-17, 74046-002-13, 74046-002-14, 74046-002-19, 74046-002-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
GLYCERINPDC6A3C0OXIACT
METHYL BENZOATE6618K1VJ9TIACT
SILVER CATION57N7B0K90AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d587a3a5-0d8c-56fd-e053-2a95a90a7725afde5a37-b3d0-23b4-e053-2a95a90aa5202022-01-14WarningsExact identifier
spl set id: afde5a37-b3d0-23b4-e053-2a95a90aa520

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.