FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Magnet Fragrance Accessories Corp | Magnet Fragrance & Accessories Corp
Effective date
2020-06-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:43

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 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#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

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

purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60mL NDC: 77707-008-01 60mL60mL

10mL NDC: 77707-009-03 10mL10mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136944348523569GTIN-13: 6944348523569
EAN-13: 6944348523569
GTIN storage (14 digits): 06944348523569		BM001-60-1.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77707-008-012022-01-28C16284748780-1d6a99b39-a8e4-a426-e053-dadaa90af4c2a81bdf7f-f324-f305-e053-2995a90a50dd
77707-008-022022-01-28C16284748780-1d6a99b39-a8e4-a426-e053-dadaa90af4c2a81bdf7f-f324-f305-e053-2995a90a50dd
77707-008-032022-01-28C16284748780-1d6a99b39-a8e4-a426-e053-dadaa90af4c2a81bdf7f-f324-f305-e053-2995a90a50dd
77707-009-012022-01-28C16284748780-1d6a99b39-a8e4-a426-e053-dadaa90af4c2a81bdf7f-f324-f305-e053-2995a90a50dd
77707-009-022022-01-28C16284748780-1d6a99b39-a8e4-a426-e053-dadaa90af4c2a81bdf7f-f324-f305-e053-2995a90a50dd
77707-009-032022-01-28C16284748780-1d6a99b39-a8e4-a426-e053-dadaa90af4c2a81bdf7f-f324-f305-e053-2995a90a50dd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77707-008-01Hand Sanitizer60 mL in 1 BOTTLELIQUID601
77707-008-02Hand Sanitizer100 mL in 1 BOTTLELIQUID1001
77707-008-03Hand Sanitizer300 mL in 1 BOTTLELIQUID3001
77707-009-01Hand Sanitizer2 mL in 1 BOTTLELIQUID21
77707-009-02Hand Sanitizer5 mL in 1 BOTTLELIQUID51
77707-009-03Hand Sanitizer10 mL in 1 BOTTLELIQUID101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77707-008HAND SANITIZER (ALCOHOL) LIQUID [MAGNET FRAGRANCE ACCESSORIES CORP]1Legacy NDC, 3 package rows20200615_a81bdf7f-f324-f305-e053-2995a90a50dd.zip
77707-009HAND SANITIZER (ALCOHOL) LIQUID [MAGNET FRAGRANCE ACCESSORIES CORP]1Legacy NDC, 3 package rows20200615_a81bdf7f-f324-f305-e053-2995a90a50dd.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77707-00877707-008-01, 77707-008-02, 77707-008-03
77707-00977707-009-01, 77707-009-02, 77707-009-03

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a81bcbff-94e9-226b-e053-2995a90a4e40a81bdf7f-f324-f305-e053-2995a90a50dd2020-06-15WarningsExact identifier
spl id: a81bcbff-94e9-226b-e053-2995a90a4e40
spl set id: a81bdf7f-f324-f305-e053-2995a90a50dd

Reported adverse events (FAERS/openFDA)#

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