FDA.reportPublic FDA data

Neutrevo Liquid Hand Disinfectant

Manufacturer
SCK ZETA DIS TICARET PAZARLAMA LIMITED SIRKETI
Effective date
2022-01-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:47:28

Label at a glance#

ProductNeutrevo Liquid Hand Disinfectant
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Apply a small amount of the liquid on the palm of your hand and rub your hands until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 86 F (30 C).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol
  3. Hydrogen peroxide
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Liquid hand disinfectant to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

Avoid direct contact with eyes. Highly flammable liquid and vapour.

Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Keep container tightly closed. Use only non-sparking tools. Store in a well ventilated place. Keep cool.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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

  • Apply a small amount of the liquid on the palm of your hand and rub your hands until dry.
  • Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store below 86 F (30 C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 mL NDC: 86818-003-01

100 ml100 ml250 ml NDC 86818-003-02

250 ml250 ml500 ml NDC 86818-003-03

500 ml500 ml1000 ml NDC 86818-003-04

1000 ml1000 ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
86818-003-012024-01-30C16284748780-11030e365-63ac-111a-e063-dadaa90a10e2Neutrevo Liquid Hand Disinfectant
86818-003-022024-01-30C16284748780-11030e365-63ac-111a-e063-dadaa90a10e2Neutrevo Liquid Hand Disinfectant
86818-003-032024-01-30C16284748780-11030e365-63ac-111a-e063-dadaa90a10e2Neutrevo Liquid Hand Disinfectant
86818-003-042024-01-30C16284748780-11030e365-63ac-111a-e063-dadaa90a10e2Neutrevo Liquid Hand Disinfectant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86818-003-01Neutrevo Liquid Hand Disinfectant100 mL in 1 BOTTLE, PLASTICLIQUID1002
86818-003-02Neutrevo Liquid Hand Disinfectant250 mL in 1 BOTTLE, PLASTICLIQUID2502
86818-003-03Neutrevo Liquid Hand Disinfectant500 mL in 1 BOTTLE, PLASTICLIQUID5002
86818-003-04Neutrevo Liquid Hand Disinfectant1000 mL in 1 BOTTLE, PLASTICLIQUID10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86818-003NEUTREVO LIQUID HAND DISINFECTANT (ALCOHOL) LIQUID [SCK ZETA DIS TICARET PAZARLAMA LIMITED SIRKETI]2Legacy NDC, 4 package rows20220124_ac24598c-aaf1-95d8-e053-2995a90a42e2.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86818-00386818-003-01, 86818-003-02, 86818-003-03, 86818-003-04

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
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
d647ebd2-6f11-80dc-e053-2a95a90a1d6eac24598c-aaf1-95d8-e053-2995a90a42e22022-01-23WarningsExact identifier
spl id: d647ebd2-6f11-80dc-e053-2a95a90a1d6e
spl set id: ac24598c-aaf1-95d8-e053-2995a90a42e2

Reported adverse events (FAERS/openFDA)#

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