90018 Sanitizer Pen

Manufacturer
Huizhou Bliss Commodity Co., Ltd
Effective date
2020-09-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:26:40

Label at a glance#

Product90018 Sanitizer Pen
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (w/w)
75g/117mL

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For Hand Sanitizing

Warnings

WARNINGS SECTION

For external use only-hands.
Flammable. Keep away from heat and flame.

Keep out of reach of children.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

/

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

/

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74274-201-01 4.7312ML74274-201-01 4.7312ML

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74274-201-012024-07-30C16284748780-11030e365-43af-111a-e063-dadaa90a10e274274-201 90018 Sanitizer Pen
74274-201-012024-01-30C16284748780-11030e365-43af-111a-e063-dadaa90a10e274274-201 90018 Sanitizer Pen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74274-201-0190018 Sanitizer Pen4.7312 mL in 1 BOTTLESPRAY4.73121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74274-20190018 SANITIZER PEN SPRAY [HUIZHOU BLISS COMMODITY CO., LTD]1Legacy NDC, 1 package rows20200903_ae525bb5-bc98-6e44-e053-2995a90a04ac.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74274-20174274-201-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT

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
ae51a8ca-e292-0ca0-e053-2995a90a10cfae525bb5-bc98-6e44-e053-2995a90a04ac2020-09-02WarningsExact identifier
spl id: ae51a8ca-e292-0ca0-e053-2995a90a10cf
spl set id: ae525bb5-bc98-6e44-e053-2995a90a04ac

Reported adverse events (FAERS/openFDA)#

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