FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
ShangRao chunyu Technology CO.,LTD.
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:31:11

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Store between 15-30"C(59-86"F Avoid freezing and excessive heat above 40"C(104F

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% V/V.

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can causedisease. For use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only. Flammable, Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • on infants
    on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouthIn case of contact with eyes, rinse eyes thoroughly with wate

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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,

Directions

DOSAGE & ADMINISTRATION SECTION

  • Store between 15-30"C(59-86"F Avoid freezing and excessive heat above 40"C(104F

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water, Triethanolamine, CarbomePropylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

OTC - PURPOSE SECTION

sterilization

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

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
72922-02172922-021-01, 72922-021-02, 72922-021-03, 72922-021-04, 72922-021-05, 72922-021-06, 72922-021-07, 72922-021-08, 72922-021-09, 72922-021-10, 72922-021-11, 72922-021-12, 72922-021-13

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
CARBOMER 934Z135WT9208IACT
WATER059QF0KO0RIACT

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
b8d7de9a-05d8-6dba-e053-2995a90aeabca57cb2ca-305d-2bbc-e053-2a95a90a0b152021-01-14WarningsExact identifier
spl set id: a57cb2ca-305d-2bbc-e053-2a95a90a0b15

Reported adverse events (FAERS/openFDA)#

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