Nordland Hand Sanitizer

Manufacturer: Nordland Development, S. de R.L. de C.V.
Effective date: 2020-10-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:35:09

Label at a glance#

ProductNordland Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry Supervise children under 6 years of age when using this product to avoid swallowing

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Glycerin, distilled water, triethanolamine, carbomer and fragrance

USE(S)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If Swallowed get medical help or contact a Posion Control Center right away.

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

DO NOT USE

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rush occurs. These may be signs of a seious condition.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86°F)
Avoid freezing and excessive heat above 40°C (104°F)

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry
Supervise children under 6 years of age when using this product to avoid swallowing

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
90029-003-32	2022-01-28	C162847	48780-1	d6a99b39-e7ba-a426-e053-dadaa90af4c2	Nordland Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
90029-003-32	Nordland Hand Sanitizer	960 mL in 1 BOTTLE	GEL	960		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
90029-003	NORDLAND HAND SANITIZER (ALCOHOL) GEL [NORDLAND DEVELOPMENT, S. DE R.L. DE C.V.]	1	Legacy NDC, 1 package rows	20201215_b10145fc-5a13-4ecd-e053-2995a90a38ef.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
90029-003	90029-003-32

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
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	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
b1015090-6bb6-53e4-e053-2a95a90a2140			b10145fc-5a13-4ecd-e053-2995a90a38ef	2020-10-06	Warnings	Exact identifier spl id: b1015090-6bb6-53e4-e053-2a95a90a2140 spl set id: b10145fc-5a13-4ecd-e053-2995a90a38ef

Reported adverse events (FAERS/openFDA)#

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