Purmist

Manufacturer
MKR International Inc
Effective date
2021-02-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:38:04

Label at a glance#

ProductPurmist
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Cl 0.13%

OTC - PURPOSE SECTION


Antiseptic

INDICATIONS & USAGE SECTION

Hand sanitizing to decrease harmful bacteria on the skin. Recommended for repeated use when water and soap are not available.

WARNINGS SECTION

For external use only. Do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Spray as needed. Rub hands together covering all areas, including fingernail areas thoroughly.

INACTIVE INGREDIENT SECTION

Dimethicone, Polysorbate 80, Proprietary blend of natural botanical oils, water.

PURMIST® 7.1mL / 0.24 fl. oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN3
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD3
1049254benzalkonium chloride 0.13 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50353-105-102023-01-30C16284748780-1f386c64a-38ab-0266-e053-dadaa90a7c1aHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50353-105-10Purmist1 in 1 BLISTER PACKLIQUID13
50353-105-10Purmist7.1 mL in 1 BOTTLE, PUMPLIQUID7.13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50353-105PURMIST (BENZALKONIUM CL) LIQUID [MKR INTERNATIONAL INC]3Legacy NDC, 2 package rows20210212_958923fc-3ff8-1b38-e053-2a95a90a93ed.zip

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
50353-10550353-105-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
bb14d4ec-6382-3e01-e053-2995a90a5ebc958923fc-3ff8-1b38-e053-2a95a90a93ed2021-02-11WarningsExact identifier
spl id: bb14d4ec-6382-3e01-e053-2995a90a5ebc
spl set id: 958923fc-3ff8-1b38-e053-2a95a90a93ed

Reported adverse events (FAERS/openFDA)#

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