HUSTLE BUTTER ANTIBACTERIAL FOAMING

Product NDC: 72014-200
Requested package NDC: 72014-200-08
11-digit product format: 720140200
Labeler code: 72014
Product ID: 72014-200_1077ee97-7785-43ba-b732-d09bf59f6d87
Type: HUMAN OTC DRUG
Nonproprietary name: Benzalkonium Chloride
Dosage form: SOAP
Route: TOPICAL
Labeler: H.B.D. DIST. INC.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-05-30
Substance: BENZALKONIUM CHLORIDE
Active strength: .1 g/100mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: HUSTLE BUTTER ANTIBACTERIAL FOAMING
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BENZALKONIUM CHLORIDE	.1 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F5UM2KM3W7	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1233282	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
d35ae631-832b-4267-aa30-cabb766ebf1b	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72014-200-07	HUSTLE BUTTER ANTIBACTERIAL FOAMING	207 mL in 1 BOTTLE, PUMP	SOAP	207		3
72014-200-08	HUSTLE BUTTER ANTIBACTERIAL FOAMING	100 mL in 1 BOTTLE, PUMP	SOAP	100		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72014-200	HUSTLE BUTTER ANTIBACTERIAL FOAMING (BENZALKONIUM CHLORIDE) SOAP [H.B.D. DIST. INC.]	2	Current NDC, 2 package rows	20241009_d35ae631-832b-4267-aa30-cabb766ebf1b.zip

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
HUSTLE BUTTER ANTIBACTERIAL FOAMING	BENZALKONIUM CHLORIDE	H.B.D. DIST. INC.	d35ae631-832b-4267-aa30-cabb766ebf1b	2026-01-09	Warnings	Exact identifier ndc (package): 72014-200-08 ndc (product): 72014-200 ndc11 (package): 72014020008

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F5UM2KM3W7	BENZALKONIUM CHLORIDE	8001-54-5	BENZALKONIUM CHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	PSN	d35ae631-832b-4267-aa30-cabb766ebf1b	3
1233282	benzalkonium chloride 1 MG/ML Medicated Liquid Soap	SCD	d35ae631-832b-4267-aa30-cabb766ebf1b	3
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	SY	d35ae631-832b-4267-aa30-cabb766ebf1b	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
72014-200-08	72014020008	100 mL in 1 BOTTLE, PUMP (72014-200-08)	100 ml	2024-11-01	No	No	Current