FDA.reportPublic FDA data

Its Nanoed Hand

Manufacturer
Sawgrass Nutra Labs | RWM Technologies, LLC
Effective date
2021-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:48:23

Label at a glance#

ProductIts Nanoed Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

On dry hands, place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until hands are entirely dry.

Storage and handling

Store between 15-30 C (59-86 F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE(S)

INDICATIONS & USAGE SECTION

To help reduce bacteria that potentially can cause disease. For when soap and water are not available.

WARNINGS:

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • on 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.

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

On dry hands, place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until hands are entirely dry.

Other Information:

STORAGE AND HANDLING SECTION

Store between 15-30 C (59-86 F)

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

3-(trimethoxysilyl) propyldimethyl-octadecyl ammonium chloride, Glycerin, Water.

8HR It's Nanoed Hand Sanitizer+

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GallonGallonSee image below for content...

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81669-00181669-001-01, 81669-001-02, 81669-001-16

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
GLYCERINPDC6A3C0OXIACT
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDEIQ36O85WQ4IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
d941dd7f-1687-2870-e053-2995a90a9848bca4df40-04ba-da84-e053-2a95a90a1eac2022-03-02WarningsExact identifier
spl set id: bca4df40-04ba-da84-e053-2a95a90a1eac

Reported adverse events (FAERS/openFDA)#

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