Unscented Hand Sanitizer Gel

Manufacturer: NATURE'S FUSIONS, LLC
Effective date: 2024-08-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:17:15

Label at a glance#

ProductUnscented Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Uses: For handwashing to decrease bacteria on the skin.

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product

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

Stop use and ask a doctor if

irritation and redness develope and persist.

INACTIVE INGREDIENT SECTION

Water, distilled, Glycerin Oil, Propylene Glycol. Carbomer (Polyacrylic acid), aminomethyl propanol

INDICATIONS & USAGE SECTION

Uses: For handwashing to decrease bacteria on the skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help promptly.

OTC - PURPOSE SECTION

Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% ... Antiseptic

OTHER SAFETY INFORMATION

Other Information

Store under 105º F

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Unscented Sanitizer Gel sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73769-050-64	Unscented Hand Sanitizer Gel	1892 mL in 1 BOTTLE	GEL	1892		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73769-050	UNSCENTED HAND SANITIZER GEL (ALCOHOL) GEL [NATURE'S FUSIONS, LLC]	1	Legacy NDC, 1 package rows	20240816_1fac83c3-5eb8-5816-e063-6294a90a808b.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Unscented Hand Sanitizer Gel
ALCOHOL
WATER
PROPYLENE GLYCOL
AMINOMETHYLPROPANOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73769-050	73769-050-64

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB

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
1fac83c3-5eb9-5816-e063-6294a90a808b			1fac83c3-5eb8-5816-e063-6294a90a808b	2024-08-01	Warnings	Exact identifier spl id: 1fac83c3-5eb9-5816-e063-6294a90a808b spl set id: 1fac83c3-5eb8-5816-e063-6294a90a808b

Reported adverse events (FAERS/openFDA)#

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