FDA.reportPublic FDA data

CELGEN SAVE MY HANDS

Manufacturer
BBHC CO., LTD | STC Nara Co., Ltd
Effective date
2020-04-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:58

Label at a glance#

ProductCELGEN SAVE MY HANDS
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Put product onto palm and then rub hands together. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 77%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use on hands.

Flammable. Keep away from fire.

Warnings

OTC - DO NOT USE SECTION

Do not use in or near the eyes. In case of contact, rinse with water.

Warnings

OTC - ASK DOCTOR SECTION

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

Warnings

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.

Directions

INDICATIONS & USAGE SECTION

Put product onto palm and then rub hands together.

Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Ammonium Acryloyldimethyltaurate/VP Copolymer, Eucalyptus Globulus Leaf Oil, Aloe Barbadensis Leaf Juice, Chlorhexidine Digluconate, Sodium Chloride, Glucose

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30ml NDC: 76731-201-01 Label30ml NDC: 76731-201-01 Label

300ml NDC: 76731-201-02 Label300ml NDC: 76731-201-02 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76731-201-012022-06-15C16284748780-1d6a99b39-a4b0-a426-e053-dadaa90af4c2a41f9122-e8e1-7bb9-e053-2995a90a380b
76731-201-022022-06-15C16284748780-1d6a99b39-a4b0-a426-e053-dadaa90af4c2a41f9122-e8e1-7bb9-e053-2995a90a380b
76731-201-012022-01-28C16284748780-1d6a99b39-a4b0-a426-e053-dadaa90af4c2a41f9122-e8e1-7bb9-e053-2995a90a380b
76731-201-022022-01-28C16284748780-1d6a99b39-a4b0-a426-e053-dadaa90af4c2a41f9122-e8e1-7bb9-e053-2995a90a380b

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76731-20176731-201-01, 76731-201-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
EUCALYPTUS OIL2R04ONI662IACT
CHLORHEXIDINE GLUCONATEMOR84MUD8EIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATEKBC00G95HIIACT
SODIUM CHLORIDE451W47IQ8XIACT
ALOE VERA LEAFZY81Z83H0XIACT
ANHYDROUS DEXTROSE5SL0G7R0OKIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT

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
e176d71a-249c-4c59-e053-2995a90ad4d6a41f9122-e8e1-7bb9-e053-2995a90a380b2022-06-15WarningsExact identifier
spl set id: a41f9122-e8e1-7bb9-e053-2995a90a380b

Reported adverse events (FAERS/openFDA)#

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