STERITE NEUTRUM

Manufacturer
PALVI MEXICO, S.A. DE C.V.
Effective date
2021-02-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:39:08

Label at a glance#

ProductSTERITE NEUTRUM
Active ingredientBENZALKONIUM CHLORIDE, DIDECYLDIMONIUM CHLORIDE
Label structure10 sections

Indications and uses

USES HAND AND SURFACE DISINFECTANT TO HELP REDUCE BACTERIA THAT POTENTIALLY CAUSE DISEASES

Dosage and administration

DIRECTIONS SPRAY STERITE NEUTRUM ON 12 TO 16 INCHES OVER HANDS, RUB AND AIR DRY, ON SURFACES APPLYING A FINE MIST, WIPE CLEAN. NO RINSING REQUIRED.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

DIDECYLDIMONIUM CHLORIDE

BENZALKONIUM CHLORIDE

PURPOSE

OTC - PURPOSE SECTION

PURPOSE

ANTIMICROBIAL

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

USES

HAND AND SURFACE DISINFECTANT TO HELP REDUCE BACTERIA THAT POTENTIALLY CAUSE DISEASES

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS SPRAY STERITE NEUTRUM ON 12 TO 16 INCHES OVER HANDS, RUB AND AIR DRY, ON SURFACES APPLYING A FINE MIST, WIPE CLEAN. NO RINSING REQUIRED.

WARNINGS

WARNINGS SECTION

WARNING FOR EXTERNAL USE ONLY

WARNINGS AND PRECAUTIONS SECTION

DO NOT USE ON OPEN WOUNDS ON THE SKIN, EYES OR MUCOUS MEMBRANES

DO NOT USE IN EYES. IF CONTACT OCCURS, FLUSH THE EYES WELL WITH PLENTY OF WATER.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

STOP USE SECTION

OTC - STOP USE SECTION

STOP USE AND SEE A DOCTOR IF IRRITATION OR RASH OCCURS

THESE COULD BE SIGNS OF A SERIOUS CONDITION

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: WATER, N-NONYLPHENOL, EUCALYPTOL, DISODIUM EDTA,

PACKAGE LABEL PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

STERITE NEUTRUMSTERITE NEUTRUM

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81576-3000-22022-07-29C16284748780-1e4f33bdf-a9af-d8a0-e053-dadaa90a6e4eSTERITE NEUTRUM SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81576-3000-2STERITE NEUTRUM1000 mL in 1 BOTTLE, PLASTICLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81576-3000STERITE NEUTRUM (BENZALKONIUM CHLORIDE) LIQUID [PALVI MEXICO, S.A. DE C.V.]1Legacy NDC, 1 package rows20210325_bb81344b-5d3f-5b54-e053-2995a90aed08.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81576-300081576-3000-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
bb81344b-5d40-5b54-e053-2995a90aed08bb81344b-5d3f-5b54-e053-2995a90aed082021-02-16WarningsExact identifier
spl id: bb81344b-5d40-5b54-e053-2995a90aed08
spl set id: bb81344b-5d3f-5b54-e053-2995a90aed08

Reported adverse events (FAERS/openFDA)#

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