Hand Sanitizer

Manufacturer: Degasa, S.A. de C.V.
Effective date: 2023-11-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:59:45

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

To decrease bacteria on the skin that could disease. Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adults supervision. Not recommended for infants

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized water, Carbopol, Glycerin, Triethanolamine, Aminomethylpropanol, Fragances.

Uses

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could disease. Recommended for repeated use.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
Do not inhale or ingest.

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.
For children under 6, use only under adults supervision.
Not recommended for infants

Other information

SPL UNCLASSIFIED SECTION

- Do not store above 105° F.
- Harmful to wood finishes and plastic.

Warnings

WARNINGS SECTION

- For external use only: hands.
- Flammable, keep away from fire or flame.
- Keep out of reach of children.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67326-005-00	Hand Sanitizer	118 mL in 1 BOTTLE	GEL	118		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67326-005	HAND SANITIZER (ALCOHOL) GEL [DEGASA, S.A. DE C.V.]	2	Current NDC, Legacy NDC, 1 package rows	20231110_cb2da26b-7ffe-485b-afc9-96fa9e5b80c7.zip

Products#

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

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

Hand Sanitizer
ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
TROLAMINE
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67326-005	67326-005-00

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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hand Sanitizer	ALCOHOL	Degasa, S.A. de C.V.	cb2da26b-7ffe-485b-afc9-96fa9e5b80c7	2023-11-09	Warnings	Exact identifier ndc (package): 67326-005-00 ndc (product): 67326-005 ndc11 (package): 67326000500 spl id: 09bc4fa1-161f-e347-e063-6294a90ad9cf spl set id: cb2da26b-7ffe-485b-afc9-96fa9e5b80c7
Hand Sanitizer	ALCOHOL	Degasa, S.A. de C.V.	c93048f4-8c26-44c0-a966-7ef8662a7b31	2023-11-05	Warnings	Exact identifier ndc (product): 67326-005

Reported adverse events (FAERS/openFDA)#

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