FDA.reportPublic FDA data

SANIPRO Hand Sanitizer 70 50ml

Manufacturer
E.CIS COSMETIC.Co.,Ltd
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:17:47

Label at a glance#

ProductSANIPRO Hand Sanitizer 70 50ml
Active ingredientALCOHOL
Label structure12 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.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Active Ingredient(s)Active Ingredient(s)

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

PurposePurpose

Use

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

UseUse

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

WarningWarning

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

Do not useDo not use

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Stop use and ask a doctorStop use and ask a doctor

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of childrenKeep out of reach of children

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.

DirectionsDirections

Other information

STORAGE AND HANDLING SECTION

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

Other InformationOther Information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Aloe Barbadensis Leaf Extract, Panthenol, Sodium Hyaluronate, Salvia Officinalis (Sage) Leaf Extract

Inactive ingredientsInactive ingredients

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SANIPRO
HAND SANITIZER
WITH ALOE MOISTURIZER
SAFELY
CLEANS & CONDITIONS
PF SF
PARABEN & SULFATE FREE
1.69 FL.OZ. (50ML)

Package Label - Principal Display PanelPackage Label - Principal Display Panel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130617544582024GTIN-13: 0617544582024
EAN-13: 0617544582024
GTIN-12: 617544582024
UPC-A: 617544582024
GTIN storage (14 digits): 00617544582024		SANIPRO 70 Alcohol Gel 50ml.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73862-212-122022-01-28C16284748780-1d6a99b39-5a9e-a426-e053-dadaa90af4c2SANIPRO Hand Sanitizer 70% 50ml

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73862-212SANIPRO HAND SANITIZER 70 50ML (ETHYLE ALCOHOL) GEL [E.CIS COSMETIC.CO.,LTD]2Legacy NDC20200616_a7dc356a-7c69-eab9-e053-2995a90ad42c.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73862-21273862-212-10, 73862-212-11, 73862-212-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER 9404Q93RCW27EIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT
SAGE065C5D077JIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
HYALURONATE SODIUMYSE9PPT4THIACT
PANTHENOLWV9CM0O67ZIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT

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
41950cd6-0685-b104-e063-6294a90af7eda7dc356a-7c69-eab9-e053-2995a90ad42c2025-10-20WarningsExact identifier
spl set id: a7dc356a-7c69-eab9-e053-2995a90ad42c

Reported adverse events (FAERS/openFDA)#

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