MDF-HS

Manufacturer: Span-World LLC | Span-Wold LLC
Effective date: 2020-12-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:34:26

Label at a glance#

ProductMDF-HS

Active ingredientBENZALKONIUM CHLORIDE

Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

label

Dosage

DOSAGE & ADMINISTRATION SECTION

dosage

Warnings

WARNINGS AND PRECAUTIONS SECTION

Inactive

INACTIVE INGREDIENT SECTION

inac

Indications

INDICATIONS & USAGE SECTION

iau

Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

koor

Purpose

OTC - PURPOSE SECTION

pur

Warnings

WARNINGS SECTION

warn

RECENT MAJOR CHANGES SECTION

Display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77943-003-41	2022-01-28	C162847	48780-1	d6a99b39-6676-a426-e053-dadaa90af4c2	MDF HS Non-Alcohol Topical Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77943-003-41	MDF-HS	100 g in 1 BOTTLE	LIQUID	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77943-003	MDF-HS (NON-ALCOHOL HAND SANITIZER) LIQUID [SPAN-WORLD LLC]	2	Legacy NDC, 1 package rows	20201202_a839dcf8-4276-4db8-e053-2995a90a7fd5.zip

Products#

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

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

MDF-HS
Non-Alcohol Hand Sanitizer
BENZALKONIUM CHLORIDE
BENZALKONIUM
PEG/PPG-18/18 DIMETHICONE
GLYCERIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77943-003	77943-003-41

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
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PEG/PPG-18/18 DIMETHICONE	9H0AO7T794	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b56c7968-bc2a-7e08-e053-2a95a90ad059			a839dcf8-4276-4db8-e053-2995a90a7fd5	2020-12-01	Warnings	Exact identifier spl id: b56c7968-bc2a-7e08-e053-2a95a90ad059 spl set id: a839dcf8-4276-4db8-e053-2995a90a7fd5

Reported adverse events (FAERS/openFDA)#

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