75% Alcohol Instant hand sanitizer gel

Manufacturer
ZHEJIANG RIFESHOW COSMETICS CO.,LTD
Effective date
2020-04-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:28

Label at a glance#

Product75% Alcohol Instant hand sanitizer gel
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Effective disinfection reached 99.9%

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INDICATIONS & USAGE SECTION

SUITABLE FOR HAND SURFACE CLEANING DISINFECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

WARNINGS SECTION

1.THS PRODUCT 5 FOR EXTERNAL USE OF DISPOSABLE HAND DISINFECTION CONDENSATION, NOT FOR INTERNAL USE KEEP OUTOF REACHOF CHILDREN.
2. THS PRODUCT SLGHTLY RRTATES THE DAMAGEDSKON.
3.STORE IN SEALED, COOL, DRY PLACE.AVOID THE SUN AND INFLAMMBLE DURING TRANSPORTATION.

DOSAGE & ADMINISTRATION SECTION

LSAGE TAKE APPROPRIATE AMOUNT OF THIS PRODUCT ON THEPAIMAND THEN KNEADWPEPALMS,BACXOFHANDS, FNGERS. BACK OF RNGERS, THUMB.FINGERIPSANDWRISTS, UNIL HANDS AREDRY.

INACTIVE INGREDIENT SECTION

Deionized water
Glycerol
Carbopol 940
Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56084-001-012023-07-28C16284748780-10191ceaa-61c3-198a-e063-dbdaa90aec3ea2879876-e1e8-87be-e053-2995a90af9b9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56084-001-0175% Alcohol Instant hand sanitizer gel60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56084-00175% ALCOHOL INSTANT HAND SANITIZER GEL (SANITIZER GEL) GEL [ZHEJIANG RIFESHOW COSMETICS CO.,LTD]1Legacy NDC, 1 package rows20200409_a2879876-e1e8-87be-e053-2995a90af9b9.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
56084-00156084-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a2879876-e1e9-87be-e053-2995a90af9b9a2879876-e1e8-87be-e053-2995a90af9b92020-04-05WarningsExact identifier
spl id: a2879876-e1e9-87be-e053-2995a90af9b9
spl set id: a2879876-e1e8-87be-e053-2995a90af9b9

Reported adverse events (FAERS/openFDA)#

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