FDA.reportPublic FDA data

Merci Handy Hand Sanitizer Self-Love

Manufacturer
MERCI HANDY CORPORATION
Effective date
2022-11-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:46:10

Label at a glance#

ProductMerci Handy Hand Sanitizer Self-Love
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 67%

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), Acrylates Copolymer, Fragrance (Parfum), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Aminomethyl propanol, Maltodextrin, Mica, Potassium Sorbate, Sodium Benzoate,Alpha-Isomethyl Ionone, Hexyl Cinnamal, Limonene, Citronellol, Coumarin, Titanium Dioxide, D&C Red No. 33

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72866-012MERCI HANDY HAND SANITIZER SELF-LOVE (ALCOHOL) GEL [MERCI HANDY CORPORATION]2Legacy NDC20221130_b35f3f02-de08-07b9-e053-2995a90af5c1.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72866-01272866-012-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MALTODEXTRIN7CVR7L4A2DIACT
MICAV8A1AW0880IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
COUMARINA4VZ22K1WTIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
D&C RED NO. 339DBA0SBB0LIACT
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
ee9e0b0e-ad3f-c86b-e053-2a95a90a0732b35f3f02-de08-07b9-e053-2995a90af5c12022-11-29WarningsExact identifier
spl id: ee9e0b0e-ad3f-c86b-e053-2a95a90a0732
spl set id: b35f3f02-de08-07b9-e053-2995a90af5c1

Reported adverse events (FAERS/openFDA)#

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