FDA.reportPublic FDA data

DR JEFF Hand Sanitizer

Manufacturer
Jiefu (Ningbo, Zhejiang)Daily Chemicals Co., Ltd
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:32:49

Label at a glance#

ProductDR JEFF Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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

Storage and handling

Store below 106°F(41C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%±5

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable.Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product,do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash appears and lasts.

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

Place enough product in your palm to thoroughly spread on both hands and nub 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 106°F(41C)

May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Distilled water、Carbomer、glycerol、Aloe extract、triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label 60mllabel 60ml

label 104mllabel 104ml

label 236mllabel 236ml

label 473mllabel 473ml

label 1020mllabel 1020ml

label 3780mllabel 3780ml

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77266-00177266-001-01, 77266-001-02, 77266-001-03, 77266-001-04, 77266-001-05, 77266-001-06

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
ALOEV5VD430YW9IACT
TROLAMINE9O3K93S3TKIACT
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED)71DD5V995LIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
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
b832e265-86d1-f2a3-e053-2995a90a82cba4b5dac2-258d-e989-e053-2995a90af2c32021-01-05WarningsExact identifier
spl set id: a4b5dac2-258d-e989-e053-2995a90af2c3

Reported adverse events (FAERS/openFDA)#

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