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(from DailyMed)

HUSTLE BUTTER ANTIBACTERIAL FOAMING Benzalkonium Chloride .1 g/100mL Soap, 207 mL

by H.B.D. DIST. INC. · 207 mL in 1 BOTTLE, PUMP (72014-200-07)
NDC 72014-0200-07
🏷️ FDA NDC (as labeled) 72014-200-07 billing pads the product segment with a zero
This package
Contains207 mL Pack sizes2 compare ↓
Also comes in: 100 ml 72014-0200-08
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0360-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jul 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 72014-200-07
Product NDC 72014-200
11-digit billing NDC 72014020007
RxCUI 1233282
UNII F5UM2KM3W7
Application # 505G(a)(3)
SPL Set ID d35ae631-832b-4267-aa30-cabb766ebf1b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jul 2026)
Marketing start 2024-05-30
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 72014-200-07 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 72014-0200-07. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerH.B.D. DIST. INC.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code72014
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio3 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

Hustle Butter Antibacterial Foaming Soap is a topical cleanser containing benzalkonium chloride, an antimicrobial agent that is typically used in over-the-counter hand and body soaps. This product is marketed as an OTC monograph drug, meaning it follows FDA's established safety and effectiveness standards for antibacterial soap ingredients rather than undergoing individual product review. Benzalkonium chloride functions to reduce bacteria on the skin during washing.

Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 100 ml
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
g and h Protect Hand 1 mg/mL 10056-0026-00 Access 250 ml — — FDA listed —
Summit 367 Antibacterial Foam 1 mg/mL 23590-0200-10 R.L. 850 ml — — FDA listed —
Summit E2 1 mg/mL 23590-0300-10 R.L. 850 ml — — FDA listed —
Swisher 1 mg/mL 47593-0592-41 Ecolab 750 ml — — FDA listed —
Swisher TF 1 mg/mL 47593-0601-26 Ecolab 1000 ml — — FDA listed —
XtraCare Foam Antibacterial Hand Wash Refill Vanilla Passion Flower .5 g/444g 57337-0045-01 Rejoice 444 g — — FDA listed —
XtraCare Foam Antibacterial Hand Wash Refill Wild Berry Blast .5 g/444g 57337-0046-01 Rejoice 444 g — — FDA listed —
XtraCare Foam Antibacterial Hand Wash Vanilla Passion Flower .2 g/221g 57337-0047-01 Rejoice 221 g — — FDA listed —
XtraCare Foam Antibacterial Hand Wash Wild Berry Blast .2 g/221g 57337-0048-01 Rejoice 221 g — — FDA listed —
XtraCare Foam Antibacterial Hand Wash Pink Cherry Blossom .2 g/221g 57337-0049-01 Rejoice 221 g — — FDA listed —
XtraCare Foam Antibacterial Hand Wash Refill Pink Cherry Blossom .5 g/444g 57337-0050-01 Rejoice 444 g — — FDA listed —
SunDrops 87 1 mg/mL 63621-0387-14 Sunburst 3785 ml — — Discontinued —
WhiskCare 387 1 mg/mL 65585-0513-01 Whisk 50 ml — — FDA listed —
Algonquin HanClean Foam 1 mg/mL 65585-0520-01 Whisk 4000 ml — — FDA listed —
FOAM-BAC Antibacterial Hand 1 mg/mL 65585-0521-01 Whisk 1000 ml — — FDA listed —
Algonquin HanClean Foam 1 mg/mL 65585-0530-01 Whisk 4000 ml — — FDA listed —
WhiskCare 387 1 mg/mL 65585-0531-01 Whisk 50 ml — — FDA listed —
WhiskCare 357 1 mg/mL 65585-0557-01 Whisk 50 ml — — Discontinued —
WhiskCare 357 1 mg/mL 65585-0558-01 Whisk 50 ml — — FDA listed —
Jade Antibacterial Hand 1 mg/mL 65585-0586-01 Whisk 900 ml — — FDA listed —
Natural Extensions Antibacterial Foaming Hand 1 mg/mL 66975-0104-01 Benco 3785 ml — — FDA listed —
Aterra7 Antibacterial Foaming Hand 1 mg/mL 68306-0115-01 B4 530 ml — — FDA listed —
Aterra7 Antibacterial Foaming Hand Fragrance Free 1 mg/mL 68306-0117-01 B4 3785 ml — — FDA listed —
Germ-Free 24 Sanitizing 1 mg/mL 71884-0026-01 Enviro 245 ml — — FDA listed —
My-Shield Sanitizing 1 mg/mL 71884-0040-01 Enviro 244 ml — — FDA listed —
Doctor Inks Sanitizing 1 mg/mL 71884-0200-01 Enviro 118 ml — — FDA listed —
Hustle Butter Antibacterial Foaming .1 g/100mLthis 72014-0200-07 H.B.D. 207 ml — — Discontinued —
Lavex Foaming Antibacterial Hand 1 mg/mL 81551-0387-01 Clark 1000 ml — — FDA listed —
Foamy Blue 1 mg/mL 83188-0405-04 Pro 1000 ml — — FDA listed —
FloraMedis Hand Sanitizer .1 g/100mL 87215-0001-01 Sichuan 450 ml — — FDA listed —
fomin mini Hand Sanitizer Wipes MELON POP .1 g/100mL 85755-0002-08 Fomin 6 packets — — FDA listed —
Ops Instant Hand Sanitizer .1 g/100mL 79016-0105-12 Archer 1000 ml — — FDA listed —
fomin mini Hand Sanitizer Wipes COCO-NILLA BLISS .1 g/100mL 85755-0001-08 Fomin 6 packets — — FDA listed —
Nuvik Large Roll in Bucket Antibacterial Hand Wipes .1 g/100mL 74602-0900-80 Nuvik 1 pail — — FDA listed —
fomin mini Hand Sanitizer Wipes FRAGRANCE FREE .1 g/100mL 85755-0003-08 Fomin 6 packets — — FDA listed —
Non -Alcohol Cherry Scented Hand Sanitizer .1 g/100mL 54860-0612-01 Shenzhen 59 ml — — FDA listed —
Hand Sanitizer .1 g/100mL 77238-0231-11 DGH 30 ml — — FDA listed —
Non -Alcohol Grape Scented Hand Sanitizer .1 g/100mL 54860-0611-01 Shenzhen 59 ml — — FDA listed —
Non -Alcohol Peach Scented Hand Sanitizer .1 g/100mL 54860-0610-01 Shenzhen 59 ml — — FDA listed —
Non -Alcohol Blueberry scented Hand sanitizer .1 g/100mL 54860-0613-01 Shenzhen 59 ml — — FDA listed —
Claravie .1 g/100mL 61554-0315-41 Gentell 237 ml — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
72014-0200-07 You're viewing this 207 mL in 1 BOTTLE, PUMP (72014-200-07) 2024-05-30 Discontinued by firm
72014-0200-08 100 mL in 1 BOTTLE, PUMP (72014-200-08) 2024-11-01 Discontinued by firm

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 72014-0200-07?
NDC 72014-0200-07 contains 207 mL — 207 ml in 1 bottle, pump.
What is the difference between NDC 72014-0200-07 and NDC 72014-0200-08?
Both are HUSTLE BUTTER ANTIBACTERIAL FOAMING Benzalkonium Chloride .1 g/100mL Soap — the drug itself is identical. NDC 72014-0200-07 is the 207 mL package, while NDC 72014-0200-08 is the 100 ml package.
What NDC number is used to bill for this package of HUSTLE BUTTER ANTIBACTERIAL FOAMING Benzalkonium Chloride .1 g/100mL Soap?
Bill NDC 72014-0200-07 — the 11-digit billing format is 72014020007. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 72014-200-07, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 72014-0200-07, written without dashes as 72014020007. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 72014-0200-07, the first segment (72014) is the labeler code FDA assigned to H.B.D. DIST. INC.; the middle segment (0200) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (07) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 100 ml (72014-0200-08). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
H.B.D. DIST. INC. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 15 words ▾

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

⏱️ Dosage and Administration 20 words ▾

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

⚠️ Warnings 80 words ▾

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

📦 Storage and Handling 10 words ▾

Other information avoid exposure to direct sunlight and excessive heat.

🧪 Active Ingredient 6 words ▾

Active ingredient Benzalkonium Chloride 0.10% w/v

🧪 Inactive Ingredients 61 words ▾

Inactive ingredients 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

🎯 Purpose 2 words ▾

Purpose Antibacterial

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 72013-0933-02 · Shanghai 72014-0201-01 · H.B.D. →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.