Hand Sanitizer Santal Blanc

Manufacturer
Noshinku
Effective date
2025-12-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:30:09

Label at a glance#

ProductHand Sanitizer Santal Blanc
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Helps reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Drug Facts

DOSAGE & ADMINISTRATION SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% V/V

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin.
Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame.
For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and consult a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INSTRUCTIONS FOR USE SECTION

Place enough product in your palm to thoroughly cover your hands.
Rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature 20°-25°C (68°F - 77°F)
May discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Polysorbate 20, Fragrance, Panthenol, Allantoin, Aloe Barbadensis Leaf Juice, Cocos Nucifera (Coconut) Oil, Simmondsia Chinesis (Jojoba) Seed Oil, Argania Spinosa (Argan) Oil, Rosa Canina Fruit Oil, Citric Acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NOSHINKU_Santal-Blanc_Page_2NOSHINKU_Santal-Blanc_Page_2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850075581139GTIN-13: 0850075581139
EAN-13: 0850075581139
GTIN-12: 850075581139
UPC-A: 850075581139
GTIN storage (14 digits): 00850075581139
NOSHINKU_Santal-Blanc_Page_2.jpg
QR code linkQR Codenoshinku.com/pages/clean-startNOSHINKU_Santal-Blanc_Page_2.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73898-011-20Hand Sanitizer Santal Blanc20 mL in 1 BOTTLE, SPRAYSOLUTION201

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73898-01173898-011-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
Hand Sanitizer Santal BlancALCOHOL SOLUTIONNoshinku4692c807-268e-6477-e063-6394a90aac0a2025-12-22WarningsExact identifier
ndc (package): 73898-011-20
ndc (product): 73898-011
ndc11 (package): 73898001120
spl id: 4692c807-268f-6477-e063-6394a90aac0a
spl set id: 4692c807-268e-6477-e063-6394a90aac0a

Reported adverse events (FAERS/openFDA)#

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