FDA.reportPublic FDA data

HAND AND NATURE SANITIZER CHERRY BLOSSOM

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc.
Effective date
2020-09-25
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:14:13

Label at a glance#

ProductHAND AND NATURE SANITIZER CHERRY BLOSSOM
Active ingredientAlcohol
Label structure8 sections

Indications and uses

Apply on hands to decrease the bacteria on the skin

Dosage and administration

Rub a dime sized drop into hands.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 54.72%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Acid Red 18 (CI 16255), Aminomethyl Propanol, Ascorbyl Palmitate, Carbomer, Cellulose, Fragrance (Parfum), Glycerin, Green 3 (CI 42053), Hydroxypropyl Methylcellulose, Jojoba Esters, Lactose, Red 4 (CI 14700), Tocopheryl Acetate, Ultramarines (CI 77007), Water

PURPOSE

OTC - PURPOSE SECTION

SANITIZER

WARNINGS

WARNINGS SECTION

For external use only. Flammable.
Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Do not spray on an open flame or other ignition source. Do not pierce or burn, even after use. Protect from sunlight. Do no expose to temperatures exceeding 50°C/ 122°F.
-------------------------------------------------------------------------------------------
Do not use
• in children less than 2 months of age
• on open skin wounds
-------------------------------------------------------------------------------------------
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 a serious condition.
-------------------------------------------------------------------------------------------
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

Uses

INDICATIONS & USAGE SECTION

Apply on hands to decrease the bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

Rub a dime sized drop into hands.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-26951346-269-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT

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
b6eff84f-bd3f-40ab-b7b2-ca5577d29dcde7fe1f9f-00d5-4ce7-8a85-8e892897a1492021-12-10WarningsExact identifier
spl set id: e7fe1f9f-00d5-4ce7-8a85-8e892897a149

Reported adverse events (FAERS/openFDA)#

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