HUSTLE BUTTER NUMBING SPRAY

Manufacturer
H.B.D. D.I.S.T. INC.
Effective date
2026-08-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-01 13:03:12

Label at a glance#

ProductHUSTLE BUTTER NUMBING
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure10 sections

Indications and uses

For the temporary relief of pain.

Dosage and administration

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. • Children under 2 years of age: do not use, consult a doctor.

Storage and handling

avoid exposure to direct sunlight and excessive heat.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 4.0% w/v

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain.

Warnings

WARNINGS SECTION

For external use only

Do not use in large quantities, particularly over raw surfaces or blistered areas.

When using this product avoid contact with eyes.

Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. • Children under 2 years of age: do not use, consult a doctor.

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, Benzalkonium Chloride, Coumarin, Benzyl Benzoate, Citral, Limonene, Linalool, Vanillin

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

Vegan

cruelty free

CHILD-RESISTANT PACKAGE

PEEL AT BOTTOM CORNER FOR FULL DRUG FACTS

REAL NEVER FADES
@hustlebutterdeluxe

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HUSTLE BUTTER NUMBINGHUSTLE BUTTER NUMBING

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850010761367GTIN-13: 0850010761367
EAN-13: 0850010761367
GTIN-12: 850010761367
UPC-A: 850010761367
GTIN storage (14 digits): 00850010761367
72014203-1.jpg
QR code linkQR Codewww.instagram.com/hustlebutterdeluxe/72014203-1.jpg

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72014-20372014-203-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

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
HUSTLE BUTTER NUMBINGLIDOCAINE HYDROCHLORIDEH.B.D. D.I.S.T. INC.d7dfb312-6c80-4a2d-b8b2-d9891cb0b74e2026-08-24WarningsExact identifier
ndc (package): 72014-203-01
ndc (product): 72014-203
ndc11 (package): 72014020301
spl id: bdec7aca-0c6f-4a4c-9b19-df1a631f7946
spl set id: d7dfb312-6c80-4a2d-b8b2-d9891cb0b74e

Reported adverse events (FAERS/openFDA)#

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