FDA.reportPublic FDA data

Holiday Dust Set

Manufacturer
MERCI HANDY CORPORATION
Effective date
2024-01-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:07:50

Label at a glance#

ProductHoliday Dust Set
Active ingredientALCOHOL
Label structure25 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

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, D&C Red No. 30, D&C Red No. 33.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

(646)-358-3432

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

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, Benzyl Benzoate, Coumarin, Limonene, Geraniol, Chromium Oxide Greens, FD&C Yellow No. 5, FD&C Blue No. 1.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

(646)-358-3432

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

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, Ferric Ferrocyanide, D&C Red No. 30, FD&C Blue No. 1, D&C Red No. 33.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

(646)-358-3432

Package Labeling:72866-030-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kit02Kit02

Package Labeling:72866-031-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:72866-032-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:72866-033-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039708ethanol 67 % Topical GelPSN4
1039708ethanol 0.67 ML/ML Topical GelSCD4
1039708ethanol 67 % Topical GelSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72866-030-01Holiday Dust Set1 in 1 KITKIT14
72866-031-01Holiday Dust Set30 mL in 1 BOTTLEGEL30 mL67 mL in 100mL4
72866-032-01Holiday Dust Set30 mL in 1 BOTTLEGEL30 mL67 mL in 100mL4
72866-033-01Holiday Dust Set30 mL in 1 BOTTLEGEL30 mL67 mL in 100mL4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72866-030HOLIDAY DUST SET (ALCOHOL) KIT [MERCI HANDY CORPORATION]4Current NDC, Legacy NDC, 4 package rows20240125_a3bea733-8957-472f-9761-57a431d3759a.zip
72866-031HOLIDAY DUST SET (ALCOHOL) KIT [MERCI HANDY CORPORATION]4Unmatched20240125_a3bea733-8957-472f-9761-57a431d3759a.zip
72866-032HOLIDAY DUST SET (ALCOHOL) KIT [MERCI HANDY CORPORATION]4Unmatched20240125_a3bea733-8957-472f-9761-57a431d3759a.zip
72866-033HOLIDAY DUST SET (ALCOHOL) KIT [MERCI HANDY CORPORATION]4Unmatched20240125_a3bea733-8957-472f-9761-57a431d3759a.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72866-03072866-030-01
72866-03172866-031-01
72866-03272866-032-01
72866-03372866-033-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 64 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MANNITOL3OWL53L36AIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SUCROSEC151H8M554IACT
CORN0N8672707OIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MALTODEXTRIN7CVR7L4A2DIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
D&C RED NO. 302S42T2808BIACT
D&C RED NO. 339DBA0SBB0LIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZYL BENZOATEN863NB338GIACT
COUMARINA4VZ22K1WTIACT
LIMONENE, (+)-GFD7C86Q1WIACT
GERANIOLL837108USYIACT
CHROMIC OXIDEX5Z09SU859IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MANNITOL3OWL53L36AIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SUCROSEC151H8M554IACT
CORN0N8672707OIACT

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
Holiday Dust SetALCOHOLMERCI HANDY CORPORATIONa3bea733-8957-472f-9761-57a431d3759a2024-01-23WarningsExact identifier
ndc (package): 72866-031-01
ndc (package): 72866-033-01
ndc (package): 72866-030-01
ndc (package): 72866-032-01
ndc (product): 72866-030
ndc11 (package): 72866003301
ndc11 (package): 72866003001
ndc11 (package): 72866003201
ndc11 (package): 72866003101
spl id: 0f9f6f2e-f7fe-acda-e063-6294a90af37d
spl set id: a3bea733-8957-472f-9761-57a431d3759a

Reported adverse events (FAERS/openFDA)#

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