INSTANT HAND SANITIZER

Manufacturer
Double Body Biotech Limited
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:31

Label at a glance#

ProductINSTANT HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on skin.

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub 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.(41℃)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on skin.

WARNINGS

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact,rinse eyes thoroughly with water. Stop use and
ask doctor if irritation or rash appears and lasts. Keep out of reach for 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 rub 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.(41℃)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Alcohol, Aqua, Glycereth-26, Aloe Barbadensis Leaf Extract,Carbomer,Sodium Hydroxide.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74657-001-01INSTANT HAND SANITIZER29.5 mL in 1 BOTTLEGEL29.51
74657-001-02INSTANT HAND SANITIZER50 mL in 1 BOTTLEGEL501
74657-001-03INSTANT HAND SANITIZER59 mL in 1 BOTTLEGEL591
74657-001-04INSTANT HAND SANITIZER100 mL in 1 BOTTLEGEL1001
74657-001-05INSTANT HAND SANITIZER150 mL in 1 BOTTLEGEL1501
74657-001-06INSTANT HAND SANITIZER200 mL in 1 BOTTLEGEL2001
74657-001-07INSTANT HAND SANITIZER240 mL in 1 BOTTLEGEL2401
74657-001-08INSTANT HAND SANITIZER300 mL in 1 BOTTLEGEL3001
74657-001-09INSTANT HAND SANITIZER350 mL in 1 BOTTLEGEL3501
74657-001-10INSTANT HAND SANITIZER400 mL in 1 BOTTLEGEL4001
74657-001-11INSTANT HAND SANITIZER500 mL in 1 BOTTLEGEL5001
74657-001-12INSTANT HAND SANITIZER1000 mL in 1 BOTTLEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74657-001INSTANT HAND SANITIZER GEL [DOUBLE BODY BIOTECH LIMITED]1Legacy NDC, 12 package rows20200409_a2bffb7f-c5a4-ae54-e053-2995a90ab973.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
a2c00f0b-7438-1267-e053-2a95a90ad31ca2bffb7f-c5a4-ae54-e053-2995a90ab9732020-04-07WarningsExact identifier
spl id: a2c00f0b-7438-1267-e053-2a95a90ad31c
spl set id: a2bffb7f-c5a4-ae54-e053-2995a90ab973

Reported adverse events (FAERS/openFDA)#

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