FDA.reportPublic FDA data

CB Advanced Hand Sanitizer

Manufacturer
Cb Distributors, Inc.
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:17:17

Label at a glance#

ProductCB Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • Children under 6, use only under adult supervision.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

• to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hands thoroughly with product and allow to dry without wiping • Children under 6, use only under adult supervision.

Other Information

SPL UNCLASSIFIED SECTION

• store below 105°F • may discolor certain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

• Purified water(Aqua), Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76813-014-002023-01-30C16284748780-1f386c649-cc49-0266-e053-dadaa90a7c1aCB Advanced Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76813-014-00CB Advanced Hand Sanitizer60 mL in 1 BOTTLEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76813-014CB ADVANCED HAND SANITIZER (ALCOHOL) GEL [CB DISTRIBUTORS, INC.]2Legacy NDC, 1 package rows20200612_7277d439-79f4-434e-9dbd-2991036bb30e.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76813-01476813-014-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
EDETOLQ4R969U9FRIACT
ALCOHOL3K9958V90MACTIB

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
a7d2773d-ddd5-7472-e053-2995a90a76957277d439-79f4-434e-9dbd-2991036bb30e2020-06-11WarningsExact identifier
spl id: a7d2773d-ddd5-7472-e053-2995a90a7695
spl set id: 7277d439-79f4-434e-9dbd-2991036bb30e

Reported adverse events (FAERS/openFDA)#

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