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 23:18:33

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 could 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, Thickener, 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
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79041-001-01SENTINEL HAND SANITIZER59 mL in 1 TUBEGEL591
79041-001-02SENTINEL HAND SANITIZER75 mL in 1 TUBEGEL751
79041-001-03SENTINEL HAND SANITIZER118 mL in 1 TUBEGEL1181
79041-001-04SENTINEL HAND SANITIZER125 mL in 1 TUBEGEL1251
79041-001-05SENTINEL HAND SANITIZER236 mL in 1 TUBEGEL2361
79041-001-06SENTINEL HAND SANITIZER250 mL in 1 TUBEGEL2501
79041-001-07SENTINEL HAND SANITIZER500 mL in 1 TUBEGEL5001
79041-001-08SENTINEL HAND SANITIZER1000 mL in 1 TUBEGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79041-001SENTINEL HAND SANITIZER (ALCOHOL) GEL [DANLAB DANUTA KATRYNSKA]1Legacy NDC, 8 package rows20200623_233c3c1b-9b56-44c4-b66e-a9026027492a.zip

Products#

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

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

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
c427c609-98ad-4fda-9328-161afe7056fc233c3c1b-9b56-44c4-b66e-a9026027492a2020-06-18WarningsExact identifier
spl id: c427c609-98ad-4fda-9328-161afe7056fc
spl set id: 233c3c1b-9b56-44c4-b66e-a9026027492a

Reported adverse events (FAERS/openFDA)#

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