Zeroth premium hand sanitizer

Manufacturer
Biocleansingcompany Co., Ltd | DongbangCosmetics Co., ltd.
Effective date
2020-05-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:40

Label at a glance#

ProductZeroth premium hand sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• instant hand antiseptic to decrease bacteria on the skin

Dosage and administration

• Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry. • Supervise children in the use of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% v/v

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Carbomer, Tetrahydroxypropyl Ethylenediamine, Tocopheryl Acetate, Lavandula Angustifolia (Lavender) Oil, Fragaria Chiloensis (Strawberry) Fruit Extract, Sophora Angustifolia Root Extract, Morus Alba Bark Extract, Glycyrrhiza Uralensis (Licorice) Root Extract, Citrus Paradisi (Grapefruit) Fruit Extract, Camellia Sinensis Leaf Extract, Cnidium Officinate Rhizome Extract

Purpose

OTC - PURPOSE SECTION

Hand Sanitizer

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame
--------------------------------------------------------------------------------------------------------
Do not use
• in children less than 2 months of age
• on open skin wounds
--------------------------------------------------------------------------------------------------------
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Uses

INDICATIONS & USAGE SECTION

• instant hand antiseptic to decrease bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.
• Supervise children in the use of this product.

Other information

OTHER SAFETY INFORMATION

• Store between 1-30C (39-86F)
• Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78393-010-012022-01-28C16284748780-1d6a99b39-589f-a426-e053-dadaa90af4c28a984f5f-d3a6-458b-8b39-90767d548c0b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78393-010-01Zeroth premium hand sanitizer500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78393-010ZEROTH PREMIUM HAND SANITIZER (ALCOHOL) GEL [BIOCLEANSINGCOMPANY CO., LTD]1Legacy NDC, 1 package rows20200527_8a984f5f-d3a6-458b-8b39-90767d548c0b.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78393-01078393-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
256f2984-2afe-4ff4-acd1-4a841d185f6e8a984f5f-d3a6-458b-8b39-90767d548c0b2020-05-27WarningsExact identifier
spl id: 256f2984-2afe-4ff4-acd1-4a841d185f6e
spl set id: 8a984f5f-d3a6-458b-8b39-90767d548c0b

Reported adverse events (FAERS/openFDA)#

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