FDA.reportPublic FDA data

HUSTLE BUTTER ANTIBACTERIAL FOAMING

Manufacturer
H.B.D. DIST. INC.
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:33:22

Label at a glance#

ProductHUSTLE BUTTER ANTIBACTERIAL FOAMING
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

• for washing to decrease bacteria on the skin • recommended for repeated use

Dosage and administration

• wet the skin • apply palmful to hands • scrub thoroughly on the skin • rinse and repeat

Storage and handling

avoid exposure to direct sunlight and excessive heat.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10% w/v                                                                                          

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

• for washing to decrease bacteria on the skin • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Do not use • in the eyes • if you are allergic to any ingredients

When using this product do not use in or near the eyes. In case of contact rinse eyes thoroughly with water.

Stop use and ask a doctor if • irritation and redness develop • condition persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet the skin • apply palmful to hands • scrub thoroughly on the skin • rinse and repeat

Other information

STORAGE AND HANDLING SECTION

avoid exposure to direct sunlight and excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Coceth-7, PPG-1-PEG-9 Lauryl Glycol Ether, PEG-40 Hydrogenated Castor Oil, Soytrimonium Chloride, Fragrance (Parfum), Propylene Glycol, Glycerin, Water (Aqua), Chamomilla Recutita (Matricaria) Flower Extract, Camellia Sinensis Leaf Extract, Arnica Montana Flower Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Symphytum Officinale Leaf Extract, Rosmarinus Officinalis (Rosemary) Oil, Methylchloroisothiazolinone, Methylisothiazolinone, Benzyl Benzoate, Citronellol, Coumarin, Geraniol, Hexyl Cinnamal, Hydroxycitronellal

Questions or comments?

OTC - QUESTIONS SECTION

+1-212-505-3222 
You may also report serious side effects to this phone number.    
Mon - Fri 9AM-5PM ET                                                

SPL UNCLASSIFIED SECTION

PROFESSIONAL TATTOO CARE

Distributed by H.B.D. Dist. Inc.    
132 Crosby Street, New York, NY 10012                                                                                                     

Contact Us: info@hustlebutter.com
www. hustlebutter.com

Certified Vegan.
Cruelty Free. 

REAL NEVER FADES®

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FOAMING SOAPFOAMING SOAP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN3
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD3
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codewww.hustlebutter.com/hustle-bubbles-7-fl-oz72014-.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72014-200-07HUSTLE BUTTER ANTIBACTERIAL FOAMING207 mL in 1 BOTTLE, PUMPSOAP2073
72014-200-08HUSTLE BUTTER ANTIBACTERIAL FOAMING100 mL in 1 BOTTLE, PUMPSOAP1003

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72014-20072014-200-07, 72014-200-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ALOE VERA LEAFZY81Z83H0XIACT
COCETH-758Y261JLH5IACT
PPG-1-PEG-9 LAURYL GLYCOL ETHER5R8J43K25LIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
TRIMETHYLAMINE HYDROCHLORIDEUW38SRM77KIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CHAMOMILEFGL3685T2XIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
HAMAMELIS VIRGINIANA LEAFT07U1161SVIACT
COMFREY LEAFDG4F8T839XIACT
ROSEMARY OIL8LGU7VM393IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
BENZYL BENZOATEN863NB338GIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
COUMARINA4VZ22K1WTIACT
GERANIOLL837108USYIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT

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
f28edc8e-e4f6-4744-b057-8d13939a8c2dd35ae631-832b-4267-aa30-cabb766ebf1b2026-08-24WarningsExact identifier
spl set id: d35ae631-832b-4267-aa30-cabb766ebf1b

Reported adverse events (FAERS/openFDA)#

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