FDA.reportPublic FDA data

SENTINEL HAND SANITIZER

Manufacturer
DANLAB DANUTA KATRYNSKA
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:35

Label at a glance#

ProductSENTINEL HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

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

Storage and handling

Do not store above 105 0 F May discolor certain fabrics. Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that coucld cause disease.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only:hands.

Flammable. Keep away from heat or flame.

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.
  • Stop use and ask a doctor if
  • irritation or redness develops.
  • Condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 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 adult supervision.
  • Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 1050F
  • May discolor certain fabrics.
  • Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Isopropyl alcohol, Plant pharma glycerin, Peppermint oil.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 1Label 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79041-002-012022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-022022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-032022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-042022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-052022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-062022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-072022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0
79041-002-082022-01-28C16284748780-1d6a99b39-c36f-a426-e053-dadaa90af4c29e0979d6-4aa6-49e4-bc19-bf1600e2adb0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79041-002-01SENTINEL HAND SANITIZER59 mL in 1 TUBESPRAY591
79041-002-02SENTINEL HAND SANITIZER75 mL in 1 TUBESPRAY751
79041-002-03SENTINEL HAND SANITIZER118 mL in 1 TUBESPRAY1181
79041-002-04SENTINEL HAND SANITIZER125 mL in 1 TUBESPRAY1251
79041-002-05SENTINEL HAND SANITIZER236 mL in 1 TUBESPRAY2361
79041-002-06SENTINEL HAND SANITIZER250 mL in 1 TUBESPRAY2501
79041-002-07SENTINEL HAND SANITIZER500 mL in 1 TUBESPRAY5001
79041-002-08SENTINEL HAND SANITIZER1000 mL in 1 TUBESPRAY10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79041-002SENTINEL HAND SANITIZER (ALCOHOL) SPRAY [DANLAB DANUTA KATRYNSKA]1Legacy NDC, 8 package rows20200623_9e0979d6-4aa6-49e4-bc19-bf1600e2adb0.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
79041-00279041-002-01, 79041-002-02, 79041-002-03, 79041-002-04, 79041-002-05, 79041-002-06, 79041-002-07, 79041-002-08

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
PEPPERMINT OILAV092KU4JHIACT

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
cd6d987b-0f3a-4a12-959a-63ed836b1eef9e0979d6-4aa6-49e4-bc19-bf1600e2adb02020-06-18WarningsExact identifier
spl id: cd6d987b-0f3a-4a12-959a-63ed836b1eef
spl set id: 9e0979d6-4aa6-49e4-bc19-bf1600e2adb0

Reported adverse events (FAERS/openFDA)#

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