Hand Sanitizer

Manufacturer
Moroccanoil | Fareva Morton Grove, Inc.
Effective date
2022-12-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:30

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

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

Ethyl Alcohol 76% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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

OTC - WHEN USING SECTION

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.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

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

Ammonium polyacryloyldimethyl taurate, aqua/water/eau, argania spinosa (argan) kernel oil, benzoic acid, benzyl alcohol, C12-13 pareth-9, dehydroacetic acid, ethylhexylglycerin, hydroxypropyl guar, isopropyl myristate, isopropyl palmitate, lactic acid, palmitic acid, parfum/fragrance, phenoxyethanol, sodium hyaluronate.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 ml Box NDC: 69942-010-0550 ml Box NDC: 69942-010-0550 ml Tube NDC: 69942-010-0550 ml Tube NDC: 69942-010-05

50 ml NDC: 69942-010-05

100 ml Box NDC: 69942-010-10100 ml Box NDC: 69942-010-10

100 ml Tube NDC: 69942-010-10100 ml Tube NDC: 69942-010-10

100 ml NDC: 69942-010-10

250 ml NDC: 69942-010-25250 ml NDC: 69942-010-25

250 ml NDC: 69942-010-25

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1535597ethanol 76 % Topical GelPSN2
1535597ethanol 0.76 ML/ML Topical GelSCD2
1535597ethanol 76 % Topical GelSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69942-010-05Hand Sanitizer1 in 1 BOXGEL12
69942-010-05Hand Sanitizer50 mL in 1 TUBEGEL502
69942-010-10Hand Sanitizer100 mL in 1 TUBEGEL1002
69942-010-10Hand Sanitizer1 in 1 BOXGEL12
69942-010-25Hand Sanitizer250 mL in 1 BOTTLE, PUMPGEL2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69942-010HAND SANITIZER (ISOPROPYL ALCOHOL) GEL [MOROCCANOIL]2Legacy NDC, 5 package rows20221217_d0f1eab1-a957-4932-e053-2a95a90aff3c.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69942-01069942-010-05, 69942-010-10, 69942-010-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
efbc0ec1-c704-2b26-e053-2995a90ace8fd0f1eab1-a957-4932-e053-2a95a90aff3c2022-12-13WarningsExact identifier
spl id: efbc0ec1-c704-2b26-e053-2995a90ace8f
spl set id: d0f1eab1-a957-4932-e053-2a95a90aff3c

Reported adverse events (FAERS/openFDA)#

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