Hand sanitizer

Manufacturer
Dongguang Shuoguo Silicone Products Co., Ltd.
Effective date
2020-02-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:03:35

Label at a glance#

ProductHand sanitizer
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

Rub hands thoroughly with product and allow to dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the hands

Warnings

WARNINGS SECTION

flammable:keep away from flame or high heat.

when useing this product keep out of eyes.in case of contact flush eyes with water.

stop and ask a doctor if irritation or redness develop

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed

get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub hands thoroughly with product and allow to dry

INACTIVE INGREDIENT SECTION

Water ,Glycerin, Propylene Glycol, Carbomer, Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

22222244

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70939-002-16Hand sanitizer40 mL in 1 POUCHSWAB403
70939-002-16Hand sanitizer24 in 1 PACKAGESWAB243
70939-002-17Hand sanitizer40 mL in 1 POUCHSWAB403
70939-002-17Hand sanitizer144 in 1 PACKAGESWAB1443

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70939-002HAND SANITIZER (ALCOHOL) SWAB [DONGGUANG SHUOGUO SILICONE PRODUCTS CO., LTD.]3Legacy NDC, 4 package rows20200202_4a24cb0f-e99a-1d8a-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70939-00270939-002-16, 70939-002-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

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
9d860edc-505d-a546-e053-2a95a90aa5d44a24cb0f-e99a-1d8a-e054-00144ff88e882020-02-01WarningsExact identifier
spl id: 9d860edc-505d-a546-e053-2a95a90aa5d4
spl set id: 4a24cb0f-e99a-1d8a-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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