FDA.reportPublic FDA data

BBL Advanced Hand Sanitizer Refreshing

Manufacturer
Boston Biolabs. Inc. | DongbangCosmetics Co., ltd.
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:45

Label at a glance#

ProductBBL Advanced Hand Sanitizer Refreshing
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• Hand sanitizer to help reduce bacteria on the skin that could cause disease. • Recommended for repeated use.

Dosage and administration

• Put enough product in your palm to cover hands and rub hands together briskly until dry. • Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ALCOHOL 70% w/w

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Lavandula Angustifolia (Lavender) Oil, Butylene Glycol, Hexylene Glycol, Fragaria Chiloensis (Strawberry) Fruit Extract, Camellia Sinensis Leaf Extract

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.
--------------------------------------------------------------------------------------------------------
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

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

• Hand sanitizer to help reduce bacteria on the skin that could cause disease.

• Recommended for repeated use.

Directions

DOSAGE & ADMINISTRATION SECTION

• Put enough product in your palm to cover hands and 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 below 110°F (43°C).
• May discolor certain fabrics or surfaces.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78579-010-012022-01-28C16284748780-1d6a99b39-db47-a426-e053-dadaa90af4c2c5a48c1e-e218-4150-a933-e4e96a856007

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78579-010-01BBL Advanced Hand Sanitizer Refreshing500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78579-010BBL ADVANCED HAND SANITIZER REFRESHING (ALCOHOL) GEL [BOSTON BIOLABS. INC.]1Legacy NDC, 1 package rows20200609_c5a48c1e-e218-4150-a933-e4e96a856007.zip

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
78579-01078579-010-01

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
Water059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
LAVENDER OILZBP1YXW0H8IACT
Butylene Glycol3XUS85K0RAIACT
Hexylene GlycolKEH0A3F75JIACT
BEACH STRAWBERRY98542F2TQSIACT
GREEN TEA LEAFW2ZU1RY8B0IACT

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
66a9f952-d5c6-442a-b5c3-28066833a888c5a48c1e-e218-4150-a933-e4e96a8560072020-06-08WarningsExact identifier
spl id: 66a9f952-d5c6-442a-b5c3-28066833a888
spl set id: c5a48c1e-e218-4150-a933-e4e96a856007

Reported adverse events (FAERS/openFDA)#

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