FDA.reportPublic FDA data

Everybody Labo Instant Protective Hand Sanitizer

Manufacturer
Everybody Labo Limited | Ming Fai Innovative Skin Care Lab Limited
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:33:21

Label at a glance#

ProductEverybody Labo Instant Protective Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To help reduce bacteria on the skin.

Dosage and administration

Squeeze a significant amount in your palm and rub hands until fully dry. Rinse free.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes.
  • If contact occurs, rinse thorughly with water.

Stop using and ask a doctor if

OTC - STOP USE SECTION

  • Irritation or redness develops and lasts.

Keep out of reach of children 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze a significant amount in your palm and rub hands until fully dry.
  • Rinse free.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Polyquaternium-37, Phenoxyethanol, Melaleuca Alternifolia Leaf Oil.

Package Labeling: 50ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 300ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

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
76780-01676780-016-01, 76780-016-02, 76780-016-03

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TEA TREE OILVIF565UC2GIACT
ALCOHOL3K9958V90MACTIB

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
f7ab0403-6f33-9925-e053-6294a90a28c2b4ccea3d-1afc-4162-9849-d08df33fe4fa2023-03-24WarningsExact identifier
spl set id: b4ccea3d-1afc-4162-9849-d08df33fe4fa

Reported adverse events (FAERS/openFDA)#

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