FDA.reportPublic FDA data

Hand Sanitizer Antibacterial Gel

Manufacturer
ShangRao chunyu Technology CO.,LTD.
Effective date
2020-08-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:18:50

Label at a glance#

ProductHand Sanitizer Antibacterial Gel
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Do not store above 105℉.May discolor some fabrics. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredien

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause infection

purpose

OTC - PURPOSE SECTION


Antiseptic

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush

Thoroughly with water. Avoid contact with broken shin。

Do not inhale or ingest.

Warnings

WARNINGS SECTION

For external use only：Hands

Flammable, Keep away from fire or flame

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Stop use section

OTC - STOP USE SECTION

Stop use and ask a doctor if

Irritation and redness develop

Condition persists for more than 72 hours

DOSAGE&ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Directions : Wet hands thoroughly with product and allow to dry without wiping . children under 6 , use only under adult supervision .

STORAGE AND HANDLING SECTION

Do not store above 105℉.May discolor some fabrics.

Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer 940, Glycerin, Vitamin E

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

72922-031-09 P3780ML72922-031-09 P3780ML72922-031-06 P59ML72922-031-06 P59ML72922-031-05 3780ml72922-031-05 3780ml72922-031-02 30ML72922-031-02 30ML72922-031-01 30 ML72922-031-01 30 ML72922-031-07 P100ML72922-031-07 P100ML72922-031-03 100ml72922-031-03 100ml72922-031-08 P500ML72922-031-08 P500ML72922-031-04 500ML72922-031-04 500ML

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72922-03172922-031-03, 72922-031-04, 72922-031-01, 72922-031-05, 72922-031-06, 72922-031-07, 72922-031-02, 72922-031-08, 72922-031-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALPHA-TOCOPHEROLH4N855PNZ1IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
ALCOHOL3K9958V90MACTIB

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
b8d7c556-9a92-a906-e053-2a95a90a9a27ac82d216-1859-624b-e053-2995a90a582b2021-01-14WarningsExact identifier
spl set id: ac82d216-1859-624b-e053-2995a90a582b

Reported adverse events (FAERS/openFDA)#

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