Altrufuel Hand Sanitizer

Manufacturer
Mad Dog Concepts, LLC | GENERAL ORGANICS INC | NINGBO MEINEKE Biotech Technology Co., Ltd. | Ningbo BST Clean And Care Products Co., Ltd | Guangzhou Gotdya Fine Chemical Co., Ltd. | Shantou Jiachun Biological Technology Co., Ltd.
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:25:16

Label at a glance#

ProductAltrufuel Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry.  Children should be supervised when using hand sanitizer.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 71%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep from fire or flame.

For external use only

When using this proudct

OTC - WHEN USING SECTION

Do not use in or near the eyes, ears or mouth. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation, redness or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover hands and rub hands together briskly until dry. 

Children should be supervised when using hand sanitizer.

Other Information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Triethanolamine, Aloe, Barbadensis Gel, Glycol, Propylene, Glycerin, Carbomer

Package Labeling:(75421-000-00)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1665370ethanol 71 % Topical SolutionPSN6
1665370ethanol 0.71 ML/ML Topical SolutionSCD6
1665370ethanol 71 % Topical SolutionSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75421-000-002021-07-23C16284748780-1c7ccaba7-1c26-fd44-e053-dadaa90aa01bAltrufuel Hand Sanitizer
75421-000-012021-07-23C16284748780-1c7ccaba7-1c26-fd44-e053-dadaa90aa01bAltrufuel Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75421-000-00Altrufuel Hand Sanitizer60 mL in 1 BOTTLELIQUID606
75421-000-01Altrufuel Hand Sanitizer237 mL in 1 BOTTLELIQUID2376

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75421-000ALTRUFUEL HAND SANITIZER (ALCOHOL) LIQUID [MAD DOG CONCEPTS, LLC]6Legacy NDC, 2 package rows20200820_e6166c7f-2cd2-40a0-85b4-37fdbbb751f7.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75421-00075421-000-00, 75421-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ad3de8e1-69a3-430b-e053-2995a90a86afe6166c7f-2cd2-40a0-85b4-37fdbbb751f72020-08-19WarningsExact identifier
spl id: ad3de8e1-69a3-430b-e053-2995a90a86af
spl set id: e6166c7f-2cd2-40a0-85b4-37fdbbb751f7

Reported adverse events (FAERS/openFDA)#

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