Merci Handy Hand Sanitizer Spray SAGE and TEA TREE Purifying

Manufacturer
Merci Handy Corp
Effective date
2022-11-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:46:11

Label at a glance#

ProductMerci Handy Hand Sanitizer SAGE and TEA TREE Purifying
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), Melaleuca Alternifolia (Tea Tree) Leaf Oil, Salvia Lavandulifolia Herb Oil, Limonene, Benzyl
Benzoate, Linalool

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72866-014MERCI HANDY HAND SANITIZER SAGE AND TEA TREE PURIFYING (ALCOHOL) SPRAY [MERCI HANDY CORP]3Legacy NDC20221130_b67375c2-9ba7-0521-e053-2995a90aaa02.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
72866-01472866-014-50

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
ee9e34b9-275d-3477-e053-2995a90a0091b67375c2-9ba7-0521-e053-2995a90aaa022022-11-29WarningsExact identifier
spl id: ee9e34b9-275d-3477-e053-2995a90a0091
spl set id: b67375c2-9ba7-0521-e053-2995a90aaa02

Reported adverse events (FAERS/openFDA)#

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