FDA.reportPublic FDA data

Hand Sanitizer Moisturizing Gel

Manufacturer
Guide Energy Solutions LLC
Effective date
2021-12-28
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:46:02

Label at a glance#

ProductHand Sanitizer Moisturizing Gel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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.

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses[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

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

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

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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 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.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates copolymer, aloe barbadensis leaf juice, aminomethyl propanol, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, tocopheryl acetate, water

SPL UNCLASSIFIED SECTION

Alcohol Antiseptic 70% Topical Gel

Moisturizing Formula

Vitamin E + Aloe Vera

FRESH CITRUS

FOR EXTERNAL USE ONLY

MADE IN THE USA

Manufactured By:

Guide Solutions

9330 S. Highway 99

Prague, OK 74864

405-567-0710

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Guide1Guide1

Guide2Guide2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN6
581662ethanol 0.7 ML/ML Topical GelSCD6
581662ethanol 70 % Topical GelSY6
581662ethyl alcohol 70 % Topical GelSY6

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77042-700-012023-01-30C16284748780-1f386c64a-1c23-0266-e053-dadaa90a7c1aHAND SANITIZER MOISTURIZING GEL
77042-700-082023-01-30C16284748780-1f386c64a-1c23-0266-e053-dadaa90a7c1aHAND SANITIZER MOISTURIZING GEL
77042-700-162023-01-30C16284748780-1f386c64a-1c23-0266-e053-dadaa90a7c1aHAND SANITIZER MOISTURIZING GEL
77042-700-322023-01-30C16284748780-1f386c64a-1c23-0266-e053-dadaa90a7c1aHAND SANITIZER MOISTURIZING GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77042-700-01Hand Sanitizer Moisturizing Gel3785 mL in 1 JUGGEL37856
77042-700-08Hand Sanitizer Moisturizing Gel237 mL in 1 BOTTLEGEL2376
77042-700-16Hand Sanitizer Moisturizing Gel473 mL in 1 BOTTLEGEL4736
77042-700-32Hand Sanitizer Moisturizing Gel946 mL in 1 BOTTLEGEL9466

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77042-700HAND SANITIZER MOISTURIZING GEL (ALCOHOL) GEL [GUIDE ENERGY SOLUTIONS LLC]6Legacy NDC, 4 package rows20211230_3cd7995c-bbd6-4b62-a86f-979c5f5787fc.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77042-70077042-700-01, 77042-700-08, 77042-700-16, 77042-700-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S)T967IEU43CIACT
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT

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
7a9a74d3-f682-4f24-9d25-9f37dfdab10b3cd7995c-bbd6-4b62-a86f-979c5f5787fc2021-12-28WarningsExact identifier
spl id: 7a9a74d3-f682-4f24-9d25-9f37dfdab10b
spl set id: 3cd7995c-bbd6-4b62-a86f-979c5f5787fc

Reported adverse events (FAERS/openFDA)#

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