FDA.reportPublic FDA data

Instant Hand Sanitizer

Manufacturer
Ningbo dingchi Intelligent Manufacturing Technology Co., Ltd.
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:43

Label at a glance#

ProductInstant Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry.

Storage and handling

store at 20 C (68 to 77 F) may discolor fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin.
  • when water, soap & towel are not available.
  • recommended for repeated use

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Do not apply around eyes. Do not use in ears and mouth

When using this product

OTC - WHEN USING SECTION

When using this product,avoid contact with eyes.In case of contact flush eyes with water

OTC - STOP USE SECTION

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.Children must be supervised in use of this product

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.

Other information

STORAGE AND HANDLING SECTION

  • store at 20 C (68 to 77 F)
  • may discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Triethanolamine,Carbomer, Aloe Barbadensis Gel, Fragrance, Glycerin,

Propylene Glycol, Tocopheryl Acetate (Vitamin E).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

all labelall label

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75701-00575701-005-01, 75701-005-02, 75701-005-03, 75701-005-04, 75701-005-05, 75701-005-06, 75701-005-07, 75701-005-08, 75701-005-09, 75701-005-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL ALCOHOLLKG8494WBHIACT
CARBOMER 934Z135WT9208IACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
b8d70f56-8bf9-f5e2-e053-2a95a90afc29a4078dc6-c7bd-5dbb-e053-2a95a90a1c992021-01-14WarningsExact identifier
spl set id: a4078dc6-c7bd-5dbb-e053-2a95a90a1c99

Reported adverse events (FAERS/openFDA)#

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