BENZALKONIUM CHLORIDE

Manufacturer: CHEMCO CORPORATION
Effective date: 2020-06-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:24:37

Label at a glance#

ProductBENZALKONIUM CHLORIDE

Active ingredientBENZALKONIUM CHLORIDE

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HS LOTION32OZ

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
49283-320-13	2023-02-28	C162847	48780-1	d6a99b39-8fd9-a426-e053-dadaa90af4c2	49283-320-13
49283-320-13	2022-01-28	C162847	48780-1	d6a99b39-8fd9-a426-e053-dadaa90af4c2	49283-320-13

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

BENZALKONIUM CHLORIDE
DIMETHICONE 1000
STEARYL ALCOHOL
BENZYL ALCOHOL
SODIUM HYDROXIDE
BEHENTRIMONIUM METHOSULFATE
WATER
MELALEUCA ALTERNIFOLIA LEAF
LINALOOL, (+)-
BENZALKONIUM
SORBIC ACID
ALOE VERA LEAF
PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE
PPG-1 TRIDECETH-6
CITRAL
LIMONENE, (+)-
GERANIOL
POLYQUATERNIUM-37 (10000 MPA.S)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49283-320	49283-320-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIMETHICONE 1000	MCU2324216	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
BEHENTRIMONIUM METHOSULFATE	5SHP745C61	IACT
WATER	059QF0KO0R	IACT
MELALEUCA ALTERNIFOLIA LEAF	G43C57162K	IACT
LINALOOL, (+)-	F4VNO44C09	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
SORBIC ACID	X045WJ989B	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
PROPYLENE GLYCOL DICAPRYLATE/DICAPRATE	O4446S9CRA	IACT
PPG-1 TRIDECETH-6	1K7417JX6Q	IACT
CITRAL	T7EU0O9VPP	IACT
LIMONENE, (+)-	GFD7C86Q1W	IACT
GERANIOL	L837108USY	IACT
POLYQUATERNIUM-37 (10000 MPA.S)	41QWS48DFN	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
f57919a2-938c-5b06-e053-2995a90a74db			a8493cef-4dd4-434b-e053-2a95a90a43ee	2023-02-24		Exact identifier spl set id: a8493cef-4dd4-434b-e053-2a95a90a43ee

Reported adverse events (FAERS/openFDA)#

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