NINJA GOLDFISH HAND SANITIZER SPRAY

Manufacturer
Enviro Specialty Chemicals Inc
Effective date
2022-10-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:51:50

Label at a glance#

ProductNINJA GOLDFISH HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

Hand Sanitizer to help decrease bacteria on the skin.

Dosage and administration

Spray liberally on the palms of the hands. Rub into the skin until dry. Recommended for repeat use.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic / Hand & Skin Sanitizer

Directions:

DOSAGE & ADMINISTRATION SECTION

Spray liberally on the palms of the hands. Rub into the skin until dry. Recommended for repeat use.

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help decrease bacteria on the skin.

Warnings:

WARNINGS SECTION

Do not freeze. For external use only.

Do not use in ears, eyes or mouth.

• When using this product, avoid contact with the eyes. In case of contact, flush eyes with water.

• Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of reach of children.

• Children should be supervised when using this product.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Laureth-4, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

OTC - QUESTIONS SECTION

+1(888) 331-8332, Mon-Fri 9:00AM-5:00PM (EST)

SPL UNCLASSIFIED SECTION

WITH SOOTHING ALOE VERA

FAST ACTING 15-SECOND FORMULA

Alcohol-Free

Long-lasting, alcohol-free protection from germs 

KILLS 99.99% OF GERMS

Formulated and enhanced with
Zetrisil®

MADE IN THE USA

Distributed by: Ninja Goldfish
1007 Industrial Park
Albion, Michigan 49224
Ph: 855-ninjafish | www.ninjagf.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ESC-103ESC-103

FDA-Initiated Inactive NDC Indexing#

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
71884-10371884-103-01, 71884-103-02, 71884-103-03, 71884-103-04, 71884-103-05, 71884-103-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
4b50d1f1-cf68-443c-a3e6-fda49d17f8ef2fcd03d5-f2c0-45ca-96d9-d432a1ada6942025-05-07WarningsExact identifier
spl set id: 2fcd03d5-f2c0-45ca-96d9-d432a1ada694

Reported adverse events (FAERS/openFDA)#

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