Sanitizerx Hand Sanitizer

Manufacturer
Ganzhou Olivee Cosmetic Co., Ltd.
Effective date
2020-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:54

Label at a glance#

ProductSanitizerx Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% 

Purpose

OTC - PURPOSE SECTION

 Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potential can cause disease.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep product away from heat or flame.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of serious condition.

Other Information

  • Store between 15-30℃ (59-86℉)
  • Avoid freezing and excessive heat above 40℃ (104℉)

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat, Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56136-027-012025-01-30C16284748780-12cef2736-9e02-d83d-e063-dadaa90ab31fHAND SANITIZER
56136-027-022025-01-30C16284748780-12cef2736-9e02-d83d-e063-dadaa90ab31fHAND SANITIZER
56136-027-032025-01-30C16284748780-12cef2736-9e02-d83d-e063-dadaa90ab31fHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56136-027-01Sanitizerx Hand Sanitizer100 mL in 1 BOTTLE, SPRAYSOLUTION1001
56136-027-02Sanitizerx Hand Sanitizer100 mL in 1 BOTTLESOLUTION1001
56136-027-03Sanitizerx Hand Sanitizer300 mL in 1 BOTTLE, PUMPSOLUTION3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56136-027SANITIZERX HAND SANITIZER (ALCOHOL) SOLUTION [GANZHOU OLIVEE COSMETIC CO., LTD.]1Legacy NDC, 3 package rows20200512_da639266-7f63-463f-b78c-79ebca8bb59a.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
56136-02756136-027-01, 56136-027-02, 56136-027-03

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
8b23a21e-3e11-4230-9d31-b91b928da046da639266-7f63-463f-b78c-79ebca8bb59a2020-05-11WarningsExact identifier
spl id: 8b23a21e-3e11-4230-9d31-b91b928da046
spl set id: da639266-7f63-463f-b78c-79ebca8bb59a

Reported adverse events (FAERS/openFDA)#

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