FDA.reportPublic FDA data

90013 Hand Sanitizer

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 23:26:42

Label at a glance#

Product90013 Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Do not store above 105F. May discolor some fabrics.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol(68% w/w)
68g/112mL

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

For Hand Sanitizing

WARNINGS SECTION

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

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.

Keep out of reach of children. If swallo'Ned, get medical help or call a Poison Control Center right away.

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallo'Ned, get medical help or call a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Do not store above 105F.
May discolor some fabrics.

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Carbomer, Propylene Glycol, Sodium Hydroxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74274-200-01 60ml74274-200-01 60ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74274-200-012024-07-30C16284748780-11030e365-500f-111a-e063-dadaa90a10e274274-200 90013 Hand Sanitizer
74274-200-012024-01-30C16284748780-11030e365-500f-111a-e063-dadaa90a10e274274-200 90013 Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74274-200-0190013 Hand Sanitizer60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74274-20090013 HAND SANITIZER GEL [HUIZHOU BLISS COMMODITY CO., LTD]1Legacy NDC, 1 package rows20200903_ae5f8a72-1504-1429-e053-2995a90a46e2.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
74274-20074274-200-01

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
SODIUM HYDROXIDE55X04QC32IIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
ae5f8a72-1505-1429-e053-2995a90a46e2ae5f8a72-1504-1429-e053-2995a90a46e22020-09-02WarningsExact identifier
spl id: ae5f8a72-1505-1429-e053-2995a90a46e2
spl set id: ae5f8a72-1504-1429-e053-2995a90a46e2

Reported adverse events (FAERS/openFDA)#

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