Nordland Hand Sanitizer

Manufacturer
Nordland Development, S. de R.L. de C.V.
Effective date
2020-09-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:29:15

Label at a glance#

ProductNordland Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

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.

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 eye thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

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

Place enough product on hands to cover

  • all surfaces. Rub hand together until dry. Supervise children under 6 years of age
  • when using this product to avoid swallowing.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Glycerin, distilled water, triethanolamine, carbomer and fragrance

Package Labeling:3780ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

37803780

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90029-000-012022-01-28C16284748780-1d6a99b39-954c-a426-e053-dadaa90af4c2Nordland Hand Sanitizer
90029-000-022022-01-28C16284748780-1d6a99b39-954c-a426-e053-dadaa90af4c2Nordland Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90029-000-01Nordland Hand Sanitizer3780 mL in 1 BOTTLEGEL37802
90029-000-02Nordland Hand Sanitizer1000 mL in 1 BOTTLEGEL10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90029-000NORDLAND HAND SANITIZER (ALCOHOL) GEL [NORDLAND DEVELOPMENT, S. DE R.L. DE C.V.]2Legacy NDC, 2 package rows20200915_ac89d8f5-b3e8-6248-e053-2a95a90a395e.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90029-00090029-000-01, 90029-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
af450bb7-db90-3439-e053-2995a90aae01ac89d8f5-b3e8-6248-e053-2a95a90a395e2020-09-14WarningsExact identifier
spl id: af450bb7-db90-3439-e053-2995a90aae01
spl set id: ac89d8f5-b3e8-6248-e053-2a95a90a395e

Reported adverse events (FAERS/openFDA)#

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