Label at a glance#

ProductBAK 1 750

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Alkyl (50% C14, 40% C12, 10% C10) dimethyl benzyl ammonium chloride, 1.33 g/l. Assayed by a non-USP method.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings: Keep out of reach of children. Mixing this solution with soaps or detergents will destroy its germicidal properties.

INDICATIONS & USAGE SECTION

Uses: Intended for use as a general purpose topical antiseptic for first-aid treatment of minor cuts and abrasions.

WARNINGS SECTION

Caution: Mixing this solution with soaps or detergents will destroy its germicidal properties.

DOSAGE & ADMINISTRATION SECTION

Usage: Apply to affected area for first-aid treatment of minor cuts and abrasions. Discontinue use and get medical aid if redness, irritation or infection develops. In case of deep or puncture wounds consult a physician.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

baklabel.jpg

BAK Label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1049254	Benzalkonium (Topical)	benzalkonium chloride 1.3 MG/ML Topical Solution	SCD Active

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
12745-145-01	2024-01-30	C162847	48780-1	1030e365-0407-111a-e063-dadaa90a10e2	BAK 1:750 Label
12745-145-01	2024-01-30	C162847	48780-1	1030e365-0407-111a-e063-dadaa90a10e2	BAK 1:750 Label
12745-145-02	2024-01-30	C162847	48780-1	1030e365-0407-111a-e063-dadaa90a10e2	BAK 1:750 Label
12745-145-02	2024-01-30	C162847	48780-1	1030e365-0407-111a-e063-dadaa90a10e2	BAK 1:750 Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BENZALKONIUM CHLORIDE	ACTIVE INGREDIENT	F5UM2KM3W7	7
BENZALKONIUM	ACTIVE MOIETY	7N6JUD5X6Y	7
WATER	INACTIVE INGREDIENT	059QF0KO0R	7

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

BAK 1 750
Benzalkonium Chloride
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
12745-145	12745-145-01, 12745-145-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
15	2025-08-28	full-release	2026-06-01 01:12:12

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
BAK 1 750	BENZALKONIUM CHLORIDE	Medical Chemical Corporation	d1f06aa6-2264-4ac1-a9a4-8ca9be1c9ca8	2026-07-02	Warnings	Exact identifier ndc (package): 12745-145-01 ndc (package): 12745-145-02 ndc (product): 12745-145 ndc11 (package): 12745014501 ndc11 (package): 12745014502 spl id: 55a6cc20-503e-416a-e063-6394a90aec61 spl set id: d1f06aa6-2264-4ac1-a9a4-8ca9be1c9ca8

Reported adverse events (FAERS/openFDA)#

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

BAK 1:750 Label