Hand Sanitizer

Manufacturer
Huizhou Bliss Commodity Co., Ltd
Effective date
2020-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:26

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6 use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control Center right away.

warnings:

WARNINGS SECTION

Flamable, keep away from heat and flame

For external use only-hands

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water
  • Avoid contact with broken skin
  • Do not inhale or ingest

Stop use and ask a doctor if

skin irritation develops.

Other Information:

  • Do not  store above 105℃
  • May discolor some fabrics
  • Harmful to wood finished and plastics.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6 use only under adult supervision.
  • Not recommended for infants.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN1
247835ethanol 0.62 ML/ML Topical SolutionSCD1
247835ethanol 62 % Topical SolutionSY1
247835ethyl alcohol 62 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74274-116-01Hand Sanitizer30 mL in 1 BOTTLESOLUTION301
74274-116-02Hand Sanitizer60 mL in 1 BOTTLESOLUTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74274-116HAND SANITIZER (ALCOHOL) SOLUTION [HUIZHOU BLISS COMMODITY CO., LTD]1Legacy NDC, 2 package rows20200514_eb6a73fa-bb72-4b3b-af16-92d787f39f6d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74274-11674274-116-01, 74274-116-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
1b939b8b-8ab8-4a7d-804e-1e0db9f0305ceb6a73fa-bb72-4b3b-af16-92d787f39f6d2020-05-13WarningsExact identifier
spl id: 1b939b8b-8ab8-4a7d-804e-1e0db9f0305c
spl set id: eb6a73fa-bb72-4b3b-af16-92d787f39f6d

Reported adverse events (FAERS/openFDA)#

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