hand sanitizer gel

Manufacturer: BB17, LLC
Effective date: 2018-07-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:56:16

Label at a glance#

Producthand sanitizer gel

Active ingredientALCOHOL

Label structure10 sections

Storage and handling

Other Information: Store below 110 F.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:
Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose:
Antimicrobial

WARNINGS SECTION

WARNING:
FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. FOR EXTERNAL USE ONLY.DO NOT USE IN THE EYES.

OTC - STOP USE SECTION

DISCONTINUE USE IF IRRITATION AND REDNESS DEVELOP.
IF CONDITION PERSISTS FOR MORE THAN 72 HOURS, CONSULT A DOCTOR OR PHYSICIAN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

DOSAGE & ADMINISTRATION SECTION

Directions:
Rub into hands until dry.

INACTIVE INGREDIENT SECTION

Water, Aloe barbadenis Leaf Juice, Glycerin,Propylene Glycol, Olive Oil, Fragrance, Carbomer, Triethanolamine, FD&C Blue No.1, D&C Red No.33.

STORAGE AND HANDLING SECTION

Other Information:
Store below 110 F.

INDICATIONS & USAGE SECTION

KILLS MORE THAN 99.99% OF COMMON GERMS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ebc62596-fc97-4d03-9483-7ba095d25db7	Product name	1	20151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53603-1051-1	2020-01-31	C162847	48780-1	9d75b9d1-1272-f424-e053-dadaa90a57ce	70ed0eab-558c-93dc-e053-2a95a90ae36e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53603-1051-1	hand sanitizer gel	29.5 mL in 1 BOTTLE	GEL	29.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53603-1051	HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [BB17, LLC]	1	Legacy NDC, 1 package rows	20180714_70ed0eab-558c-93dc-e053-2a95a90ae36e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

hand sanitizer gel
ETHYL ALCOHOL
FD&C BLUE NO. 1
ALCOHOL
WATER
ALOE VERA LEAF
GLYCERIN
PROPYLENE GLYCOL
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
TROLAMINE
D&C RED NO. 33
OLIVE OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
53603-1051	53603-1051-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
FD&C BLUE NO. 1	H3R47K3TBD	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	IACT
TROLAMINE	9O3K93S3TK	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
OLIVE OIL	6UYK2W1W1E	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
70ed0eab-558d-93dc-e053-2a95a90ae36e			70ed0eab-558c-93dc-e053-2a95a90ae36e	2018-07-13	Warnings	Exact identifier spl id: 70ed0eab-558d-93dc-e053-2a95a90ae36e spl set id: 70ed0eab-558c-93dc-e053-2a95a90ae36e

Reported adverse events (FAERS/openFDA)#

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