ZATURAL HAND SANITIZER

Manufacturer
Prospinach, LLC
Effective date
2022-01-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:05

Label at a glance#

ProductZATURAL HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information: Store under 105º F

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose

Antibacterial

INDICATIONS & USAGE SECTION

Uses: For hand washing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings: Flammable. Keep way from fire or flame. For external use only.

When using this product:  • Do not use in eyes. In case of contact with eyes, rinse with water.
Stop use and ask a doctor if Irritation and redness develop and persist

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children If swallowed, get medical help promptly.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry without wiping.

STORAGE AND HANDLING SECTION

Other information:

Store under 105º F

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Dimethicone Copolyol, Carbomer, Aloe Barbadensis Leaf Juice, Triethanolamine, CBD, 100% pure, undiluted essential oils of: Clove Bud, Lemon, Cinnamon Bark, Peppermint, Eucalyptus, Rosemary, Thyme

SPL UNCLASSIFIED SECTION

ADVANCED FORMULA

KILLS 99.9% OF GERMS*

Antibacterial
•70% Ethyl alcohol from corn

Antiviral*
•Powerful essential oil with antiviral properties


Immune Boost*
•Hemp has been shown to assist in boosting the immune system

Soothing
•Aloe Vera has the proven properties that soothe and protect the skin.

*Effective at eliminating 99.9% of most common, harmful germs and bacteria in as little as 15 seconds. Hand sanitizer base is manufactured in an FDA audited Drug facility to ensure quality and consistency. This product is not intended to diagnose, treat, cure or prevent any disease.

Manufactured by: ZATURAL

(208)969-1282  info@zatural.com
1150 E 990 S Eden ID 83325
FOLLOW US @zatural Instagram, Facebook, Youtube

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77615-100-01ZATURAL HAND SANITIZER3.79 L in 1 BOTTLELIQUID3.792
77615-100-02ZATURAL HAND SANITIZER0.059 L in 1 BOTTLELIQUID0.0592
77615-100-05ZATURAL HAND SANITIZER18.93 L in 1 CONTAINERLIQUID18.932
77615-100-08ZATURAL HAND SANITIZER0.237 L in 1 BOTTLELIQUID0.2372
77615-100-16ZATURAL HAND SANITIZER0.473 L in 1 BOTTLELIQUID0.4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77615-100ZATURAL HAND SANITIZER (ETHYL ALCOHOL) LIQUID [PROSPINACH, LLC]2Legacy NDC, 5 package rows20220118_66f8bf94-1101-4255-9efe-3fb725dcfb28.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77615-10077615-100-02, 77615-100-08, 77615-100-16, 77615-100-01, 77615-100-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
08c4e47a-47e8-4581-9ff1-3f1f8f014ad566f8bf94-1101-4255-9efe-3fb725dcfb282022-01-17WarningsExact identifier
spl id: 08c4e47a-47e8-4581-9ff1-3f1f8f014ad5
spl set id: 66f8bf94-1101-4255-9efe-3fb725dcfb28

Reported adverse events (FAERS/openFDA)#

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