Merci Handy Sanctuary Hand Sanitizer ARIES

Manufacturer
MERCI HANDY CORPORATION
Effective date
2022-12-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:51:59

Label at a glance#

ProductMerci Handy Sanctuary Hand Sanitizer ARIES
Active ingredientALCOHOL
Label structure8 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% (v/v)

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 the 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

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, FD&C Red No.4, D&C Red No.33, D&C Red No.30

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

(646)-358-3432

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ARIESARIES

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039708ethanol 67 % Topical GelPSN2
1039708ethanol 0.67 ML/ML Topical GelSCD2
1039708ethanol 67 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72866-018-012024-01-30C16284748780-11030e365-2e37-111a-e063-dadaa90a10e2Merci Handy Sanctuary Hand Sanitizer ARIES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72866-018-01Merci Handy Sanctuary Hand Sanitizer ARIES30 mL in 1 BOTTLEGEL302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72866-018MERCI HANDY SANCTUARY HAND SANITIZER ARIES (ALCOHOL) GEL [MERCI HANDY CORPORATION]2Legacy NDC, 1 package rows20221202_bfcd86f2-17a5-a5a8-e053-2995a90ac1dd.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72866-01872866-018-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Merci Handy Sanctuary Hand Sanitizer ZODIAC SETALCOHOLMERCI HANDY CORPORATIONbfcd01f3-4a7b-263a-e053-2a95a90aa1d42024-01-23WarningsExact identifier
ndc (package): 72866-018-01
ndc11 (package): 72866001801
eec7ceca-09aa-d877-e053-2995a90a2facbfcd86f2-17a5-a5a8-e053-2995a90ac1dd2022-12-01WarningsExact identifier
spl id: eec7ceca-09aa-d877-e053-2995a90a2fac
spl set id: bfcd86f2-17a5-a5a8-e053-2995a90ac1dd

Reported adverse events (FAERS/openFDA)#

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