FDA.reportPublic FDA data

HAND SANITIZER Cherie Cherry

Manufacturer
Merci Handy Corporation
Effective date
2022-11-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:46:10

Label at a glance#

ProductHAND SANITIZER Cherie Cherry
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%

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), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Eugenol, Coumarin, Isoeugenol, Limonene, 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

LabelLabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72866-010HAND SANITIZER CHERIE CHERRY (ALCOHOL) GEL [MERCI HANDY CORPORATION]3Legacy NDC20221130_ad282c5a-814f-49b0-e053-2995a90a6543.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72866-01072866-010-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MANNITOL3OWL53L36AIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SUCROSEC151H8M554IACT
CORN0N8672707OIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MALTODEXTRIN7CVR7L4A2DIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
EUGENOL3T8H1794QWIACT
COUMARINA4VZ22K1WTIACT
ISOEUGENOL5M0MWY797UIACT
LIMONENE, (+)-GFD7C86Q1WIACT
FD&C RED NO. 4X3W0AM1JLXIACT
D&C RED NO. 339DBA0SBB0LIACT
D&C RED NO. 302S42T2808BIACT
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
eea0755b-e10e-6af2-e053-2995a90a3400ad282c5a-814f-49b0-e053-2995a90a65432022-11-29WarningsExact identifier
spl id: eea0755b-e10e-6af2-e053-2995a90a3400
spl set id: ad282c5a-814f-49b0-e053-2995a90a6543

Reported adverse events (FAERS/openFDA)#

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