FDA.reportPublic FDA data

mPulse Antimicrobial Hand Sanitizer

Manufacturer
ANTIMICROBIAL SOLUTIONS, LLC
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:44

Label at a glance#

ProductmPulse Antimicrobial Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Helps reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Apply product to hands and rub until dry.

Storage and handling

Store in cool dry place between 35° and 103°F.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Uses

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.
  • Avoid contact with eyes.
  • In case of contact, flush thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply product to hands and rub until dry.

Other information

STORAGE AND HANDLING SECTION

Store in cool dry place between 35° and 103°F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Propylene Glycol, Triethylene Glycol, Phospholipids Complex, Organo Silane Quaternaries.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD1
1049254benzalkonium chloride 0.13 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78941-001-012022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-022022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-032022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-042022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-052022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-062022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-072022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-082022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e
78941-001-092022-01-28C16284748780-1d6a99b39-f6c1-a426-e053-dadaa90af4c27852db3a-c0ed-4976-ab63-de32fe17d25e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78941-001-01mPulse Antimicrobial Hand Sanitizer0.059 L in 1 BOTTLELIQUID0.0591
78941-001-02mPulse Antimicrobial Hand Sanitizer0.236 L in 1 BOTTLELIQUID0.2361
78941-001-03mPulse Antimicrobial Hand Sanitizer0.355 L in 1 BOTTLELIQUID0.3551
78941-001-04mPulse Antimicrobial Hand Sanitizer0.473 L in 1 BOTTLELIQUID0.4731
78941-001-05mPulse Antimicrobial Hand Sanitizer0.946 L in 1 BOTTLELIQUID0.9461
78941-001-06mPulse Antimicrobial Hand Sanitizer3.785 L in 1 JUGLIQUID3.7851
78941-001-07mPulse Antimicrobial Hand Sanitizer18.927 L in 1 JUGLIQUID18.9271
78941-001-08mPulse Antimicrobial Hand Sanitizer208.198 L in 1 DRUMLIQUID208.1981
78941-001-09mPulse Antimicrobial Hand Sanitizer1040.990 L in 1 CONTAINERLIQUID1040.9901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78941-001MPULSE ANTIMICROBIAL HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [ANTIMICROBIAL SOLUTIONS, LLC]1Legacy NDC, 9 package rows20200624_7852db3a-c0ed-4976-ab63-de32fe17d25e.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78941-00178941-001-01, 78941-001-02, 78941-001-03, 78941-001-04, 78941-001-05, 78941-001-06, 78941-001-07, 78941-001-08, 78941-001-09

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TRIETHYLENE GLYCOL3P5SU53360IACT

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
1bf327f2-190f-4e33-9e57-cf080a1fb35e7852db3a-c0ed-4976-ab63-de32fe17d25e2020-06-16WarningsExact identifier
spl id: 1bf327f2-190f-4e33-9e57-cf080a1fb35e
spl set id: 7852db3a-c0ed-4976-ab63-de32fe17d25e

Reported adverse events (FAERS/openFDA)#

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