ResQue1st Hand Sanitizer

Manufacturer
RESQUE1ST LLC
Effective date
2020-08-10
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-05-31 23:24:16

Label at a glance#

ProductResQue1st Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands and rub hands together until dry. Children under 6 years should be supervised when using this product.

Storage and handling

Store at a temperature below 110°F (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

ResQue1st Hand Sanitizer Gel

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from source of heat, fire or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and lasts.

Keep out of reach of children

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

  • Place enough product in your palm to thoroughly cover your hands and rub hands together until dry.
  • Children under 6 years should be supervised when using this product.

Storage

STORAGE AND HANDLING SECTION

  • Store at a temperature below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerine, Hydroxyethylcellulose, Purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

32 Label32 Label16 Label16 Label8 Label8 Label4 Label4 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN12
581662ethanol 0.7 ML/ML Topical GelSCD12
581662ethanol 70 % Topical GelSY12
581662ethyl alcohol 70 % Topical GelSY12

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73762-100-10ResQue1st Hand Sanitizer3790 mL in 1 JUGGEL379012
73762-100-11ResQue1st Hand Sanitizer118 mL in 1 BOTTLEGEL11812
73762-100-23ResQue1st Hand Sanitizer237 mL in 1 BOTTLEGEL23712
73762-100-47ResQue1st Hand Sanitizer473 mL in 1 BOTTLEGEL47312
73762-100-94ResQue1st Hand Sanitizer946 mL in 1 BOTTLEGEL94612

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73762-100RESQUE1ST HAND SANITIZER (ALCOHOL) GEL [RESQUE1ST LLC]12Legacy NDC, 5 package rows20200811_a5a1c5c8-acc3-fe29-e053-2995a90a314d.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73762-10073762-100-10, 73762-100-11, 73762-100-23, 73762-100-47, 73762-100-94

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML · Source PDF

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
ac8c7c6b-323e-0c88-e053-2a95a90a9859a5a1c5c8-acc3-fe29-e053-2995a90a314d2020-08-10WarningsExact identifier
spl id: ac8c7c6b-323e-0c88-e053-2a95a90a9859
spl set id: a5a1c5c8-acc3-fe29-e053-2995a90a314d

Reported adverse events (FAERS/openFDA)#

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