Eddie's Spray Hand Sanitizer 8oz Nutralife

Manufacturer
Nutralife Biosciences, Inc.
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:07:26

Label at a glance#

ProductEddies Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Indications and uses

To help reduce bacteria on the skin. 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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin. 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

-On children less than 2 months of age- On open skin wounds -around eyes -in ears and mouth

When using this product

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. -avoid contact with broken skin. - do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or rash occurs

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

-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

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (leaf) Extract, Glycerin, Fragrance, Purified water

Eddie's Clean Hands Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer 8ozHand Sanitizer 8oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1598066isopropyl alcohol 75 % Topical SprayPSN2
1598066isopropyl alcohol 0.75 ML/ML Topical SpraySCD2
1598066isopropyl alcohol 75 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73761-101-02Eddies Hand Sanitizer237 mL in 1 BOTTLESPRAY2372
73761-101-08Eddies Hand Sanitizer237 mL in 1 BOTTLESPRAY2372
73761-101-60Eddies Hand Sanitizer60 mL in 1 BOTTLESPRAY602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73761-101EDDIES HAND SANITIZER (ALCOHOL 75%) SPRAY [NUTRALIFE BIOSCIENCES, INC.]2Legacy NDC, 3 package rows20200423_a1b2c7bf-3143-d786-e053-2a95a90a1464.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73761-10173761-101-08, 73761-101-02, 73761-101-60

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
a3cf480e-2131-bbbf-e053-2995a90a1ceea1b2c7bf-3143-d786-e053-2a95a90a14642020-04-21WarningsExact identifier
spl id: a3cf480e-2131-bbbf-e053-2995a90a1cee
spl set id: a1b2c7bf-3143-d786-e053-2a95a90a1464

Reported adverse events (FAERS/openFDA)#

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