Hand Sanitizer

Manufacturer: BBC GROUP LIMITED
Effective date: 2020-07-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:20:06

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand-washing to help decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire and flames.

When using this product

OTC - WHEN USING SECTION

■ do not get into eyes.

■ if contact occurs, rinse eyes throughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develops and persists.

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylates Crosspolymer, Sodium Hydroxide, Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Yellow 5, Blue 1

Inner Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

inner package label

Blister Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

outer package label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247835	ethanol 62 % Topical Solution	PSN	1
247835	ethanol 0.62 ML/ML Topical Solution	SCD	1
247835	ethanol 62 % Topical Solution	SY	1
247835	ethyl alcohol 62 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76383-086-50	2022-01-28	C162847	48780-1	d6a99b39-7670-a426-e053-dadaa90af4c2	BBC K7 Aloe Hand Sanitizer 62 Blstr

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76383-086-02	Hand Sanitizer	50 mL in 1 BOTTLE, PLASTIC	LIQUID	50		1
76383-086-50	Hand Sanitizer	6 in 1 BLISTER PACK	LIQUID	6		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76383-086	HAND SANITIZER (ALCOHOL) LIQUID [BBC GROUP LIMITED]	1	Legacy NDC, 2 package rows	20200704_a98f175e-eaaf-4e3d-e053-2a95a90a6b7a.zip

Products#

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

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

Hand Sanitizer
Alcohol
ALOE VERA LEAF
GLYCERIN
WATER
DENATONIUM BENZOATE
FD&C BLUE NO. 1
POLYOXYL 40 HYDROGENATED CASTOR OIL
SODIUM HYDROXIDE
FD&C YELLOW NO. 5

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76383-086	76383-086-02, 76383-086-50

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
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a98f008f-80cd-d275-e053-2a95a90a4aa0			a98f175e-eaaf-4e3d-e053-2a95a90a6b7a	2020-07-03	Warnings	Exact identifier spl id: a98f008f-80cd-d275-e053-2a95a90a4aa0 spl set id: a98f175e-eaaf-4e3d-e053-2a95a90a6b7a

Reported adverse events (FAERS/openFDA)#

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