Merci Handy Hand Sanitizer Spray Lavender & Eucalyptus Relaxing

Manufacturer
Merci Handy Corp
Effective date
2022-11-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:46:11

Label at a glance#

ProductMerci Handy Hand Sanitizer Lavender and Eucalyptus Relaxing
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

in the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop 
  • condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

store at a temperature below 110° F (43° C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Fragrance (Parfum), Eucalyptus Globulus Leaf/Twig Oil, Lavandula Angustifolia (Lavender) Oil, Linalool, Limonene,  Geraniol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72866-016MERCI HANDY HAND SANITIZER LAVENDER AND EUCALYPTUS RELAXING (ALCOHOL) SPRAY [MERCI HANDY CORP]2Legacy NDC20221130_b8294f3b-05e7-5fc0-e053-2995a90aa36a.zip

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
72866-01672866-016-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ee9e1f7f-d466-1538-e053-2a95a90a7efcb8294f3b-05e7-5fc0-e053-2995a90aa36a2022-11-29WarningsExact identifier
spl id: ee9e1f7f-d466-1538-e053-2a95a90a7efc
spl set id: b8294f3b-05e7-5fc0-e053-2995a90aa36a

Reported adverse events (FAERS/openFDA)#

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