FDA.reportPublic FDA data

ANTI-BACTERIAL DAYOFF HAND SANITIZER

Manufacturer
GHOST STORIES | Natural Korea Co., Ltd.
Effective date
2022-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:49:16

Label at a glance#

ProductANTI-BACTERIAL DAYOFF HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Decrease bacteria on hands.

Dosage and administration

Rub a dime size drop into hands.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Decrease bacteria on hands.

Warnings

WARNINGS SECTION

Flammable: Keep away from heat of flame.

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On damaged skin or broken skin

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation and redness develop or increase.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Cente right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub a dime size drop into hands.

Other information

OTHER SAFETY INFORMATION

Avoid freezing and excessive heat above 40 °C (104 °F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Fragrance (Parfum), Carbomer, Lactose, Cellulose, Propylene Glycol, Hydroxypropyl Methylcellulose, Aminomethyl Propanol, L-Menthol, Jojoba Esters, Tocopheryl Acetate, Ascorbyl Palmitate, Mentha Piperita (Peppermint), Leaf Extract, Pinus Densiflora Leaf Extract, FD&C Yellow No. 5, FD&C Blue No. 1, Ultramarines.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DAYOFFDAYOFF

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82697-221-012023-07-28C16284748780-10191ceaa-6e7b-198a-e063-dbdaa90aec3e82697-221-01 | ANTI-BACTERIAL DAYOFF HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82697-221-01ANTI-BACTERIAL DAYOFF HAND SANITIZER220 mL in 1 BOTTLE, PUMPGEL2201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82697-221ANTI-BACTERIAL DAYOFF HAND SANITIZER (ALCOHOL) GEL [GHOST STORIES]1Legacy NDC, 1 package rows20220421_dc947583-e4d5-edc6-e053-2995a90ad0d4.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
82697-22182697-221-01

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
FD&C BLUE NO. 1H3R47K3TBDIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
HYDROGENATED JOJOBA OIL, RANDOMIZEDQ47ST02F58IACT
MENTHA PIPERITA LEAFA389O33LX6IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
ULTRAMARINE BLUEI39WR998BIIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
LEVOMENTHOLBZ1R15MTK7IACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
ASCORBYL PALMITATEQN83US2B0NIACT
PINUS DENSIFLORA LEAFQ1Q9P50WIYIACT
POWDERED CELLULOSESMD1X3XO9MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT

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
dc947583-e4d6-edc6-e053-2995a90ad0d4dc947583-e4d5-edc6-e053-2995a90ad0d42022-04-13WarningsExact identifier
spl id: dc947583-e4d6-edc6-e053-2995a90ad0d4
spl set id: dc947583-e4d5-edc6-e053-2995a90ad0d4

Reported adverse events (FAERS/openFDA)#

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