FDA.reportPublic FDA data

90013 Hand Sanitizer

Manufacturer
Huizhou Bliss Commodity Co., Ltd
Effective date
2020-04-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:43

Label at a glance#

Product90013 Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 68%

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 wieh 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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, glycerin, carbomer, propyene glycol, sodium hydroxide

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286291ethanol 68 % Topical SolutionPSN1
2286291ethanol 0.68 ML/ML Topical SolutionSCD1
2286291ethanol 68 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74274-009-012024-07-30C16284748780-11030e365-24ac-111a-e063-dadaa90a10e28668a08e-f08c-4720-bd44-2e2568ecba40
74274-009-012024-01-30C16284748780-11030e365-24ac-111a-e063-dadaa90a10e28668a08e-f08c-4720-bd44-2e2568ecba40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74274-009-0190013 Hand Sanitizer60 mL in 1 BOTTLESOLUTION601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74274-00990013 HAND SANITIZER (ALCOHOL) SOLUTION [HUIZHOU BLISS COMMODITY CO., LTD]1Legacy NDC, 1 package rows20200418_8668a08e-f08c-4720-bd44-2e2568ecba40.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74274-00974274-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM HYDROXIDE55X04QC32IIACT

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
5e6ca6c1-3f22-4978-bd82-878c1d5f39cb8668a08e-f08c-4720-bd44-2e2568ecba402020-04-18WarningsExact identifier
spl id: 5e6ca6c1-3f22-4978-bd82-878c1d5f39cb
spl set id: 8668a08e-f08c-4720-bd44-2e2568ecba40

Reported adverse events (FAERS/openFDA)#

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