Home › NDC Lookup › Ingredients › Benzalkonium Chloride › 83004-0033-01
🧼image loading
(from DailyMed)

Terramed Just Think Comfort Armor Antibacterial Cleansing Bar BENZALKONIUM CHLORIDE .13 g/100g Soap, 120 g

by Rida LLC · 1 BOX in 1 CARTON (83004-033-01) / 120 g in 1 BOX
NDC 83004-0033-01
🏷️ FDA NDC (as labeled) 83004-033-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ 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 ↗

🆔 Identity & classification

FDA NDC (as labeled) 83004-033-01
Product NDC 83004-033
11-digit billing NDC 83004003301
RxCUI 2057666
UNII F5UM2KM3W7
Application # M003
SPL Set ID 68e59a77-6a0c-42e2-a6a9-1353470d2e08
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-04
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 83004-033-01 — 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 → 83004-0033-01. 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

LabelerRida LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code83004
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio47 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?

This is an over-the-counter antibacterial soap bar for topical cleansing. It contains benzalkonium chloride, a quaternary ammonium compound that functions as an antimicrobial agent commonly included in cleansing products to reduce bacteria on the skin. The product is marketed under the FDA's OTC monograph rules for antiseptic cleansing agents rather than as an individually approved application.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 2P3VWU3H10
    Activated charcoal is a highly porous carbon material processed to increase its surface area. It's used in medicines as an absorbent to help bind and remove unwanted substances in the digestive system.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII R6Q3791S76
    Sodium gluconate is a salt derived from gluconic acid, a naturally occurring compound. In medicines, it functions as a buffering agent to help maintain stable pH and as a chelating agent that can bind minerals in formulations.
  • UNII 6H91L1NXTW
    A processed palm kernel oil derivative used as an emulsifier and surfactant in medications. It helps mix oil and water-based ingredients together and improves how the medicine spreads and dissolves in the body.
  • UNII S0A6004K3Z
    Sodium palmate is a salt made from palm oil. It acts as an emulsifier and surfactant in medicines, helping mix ingredients that normally don't blend well together and improving product texture and consistency.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

19 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesSodium Palmate, Sodium Palm Kernelate, Aqua (Water), Glycerin, Charcoal Powder, Mel (Manuka Honey) Extract, Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricaria) Flower Extract, Calendula Officinalis Flower Extract, Tocopheryl Acetate, Citric Acid, Fragrance, Sodium Chloride, Sodium Gluconate, Titanium Dioxide, Phenoxyethanol, Ethylhexylglycerin.

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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.
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
Covex Antibacterial Bar Active Protection 1.3 mg/g 51209-0017-00 DALAN 115 g — — FDA listed —
Covex Antibacterial Bar Cool Protection 1.3 mg/g 51209-0018-00 DALAN 115 g — — FDA listed —
Covex Antibacterial Bar Fresh Protection 1.3 mg/g 51209-0020-27 DALAN 270 g — — FDA listed —
Covex Antibacterial Bar Active Protection 1.3 mg/g 51209-0021-27 DALAN 270 g — — FDA listed —
Covex Antibacterial Bar Cool Protection 1.3 mg/g 51209-0022-27 DALAN 270 g — — FDA listed —
American Red Cross Antibacterial Bar 1.3 mg/g 51628-0034-00 My 85 g — — FDA listed —
Dove .13 g/100g 64942-1846-01 Conopco 212 g — — FDA listed —
Dove .13 g/100g 64942-2455-01 Conopco 106 g — — FDA listed —
Dove .13 g/100g 64942-2468-01 Conopco 850 g — — FDA listed —
Terramed Just Think Comfort Armor Antibacterial Cleansing Bar .13 g/100gthis 83004-0033-01 Rida 120 g — — FDA listed —
Antibacterial Wet Wipes .13 g/100g 70412-0500-10 Zhejiang 10 patches — — FDA listed —
FIRSTAR BZK Antiseptic Towelette .13 g/100g 71734-0111-01 JIANGMEN 2 g — — FDA listed —
Antibacterial Wet Wipes .13 g/100g 73015-0001-01 HangZhou 15 pouches — — FDA listed —
Antibacterial Wipes .13 g/100g 81079-0001-01 SHAOXING 38 g — — FDA listed —
Biopure Anti-bacterial Hand Wipes Fresh Morning Breeze Scent .13 g/100g 78691-0032-00 Quest 20 g — — FDA listed —
Klean Freak .13 g/100g 78982-0002-01 KLEAN 4 g — — FDA listed —
Zoviro .13 g/100g 83814-0003-01 Zoviro, 80 pouches — — FDA listed —
Zehn Antiseptic Sanitizing Wipes .13 g/100g 84488-0002-01 Zehn 1500 patches — — FDA listed —
SimplyGreat Antibacterial wet wipes .13 g/100g 85057-0001-01 Simply 40 patches — — FDA listed —
Clorox Hand Sanitizer .13 g/100g 69540-0036-01 Brand 20 patches — — Discontinued —
Hand Wipes .13 g/100g 77677-0013-20 Advanced 20 packets — — FDA listed —
Zoviro .13 g/100g 83814-0001-01 Zoviro, 20 pouches — — FDA listed —
Sipa HAND SANITIZING WIPES .13 g/100g 85137-0001-01 Sipa 50 patches — — FDA listed —
Value Wipes .13 g/100g 72202-0013-80 Zogics, 800 packets — — FDA listed —
Sanitizing Wipes .13 g/100g 72202-0200-01 Zogics, 2000 packets — — FDA listed —
Zehn Antiseptic Sanitizing Wipes .13 g/100g 84488-0001-01 Zehn 10 patches — — FDA listed —
MedPride Bath Wipes .13 g/100g 52410-4107-07 Shield 13 g — — FDA listed —
Sanitex Antibacterial Hand Wipes Fresh Scent .13 g/100g 53118-0002-01 Precare 1 canister — — FDA listed —
MediChoice Cleansing .13 g/100g 39892-0305-01 O&M 1000 patches — — FDA listed —
Klean Freak .13 g/100g 78982-0004-01 KLEAN 4 g — — FDA listed —
Biopure20Ct Anti Bacterial Hand Wipes .13 g/100g 79794-0114-01 Zhejiang 480 patches — — FDA listed —
MediChoice BZK Antiseptic .13 g/100g 39892-0304-01 O&M 1000 patches — — FDA listed —
Antibacterial Wipes .13 g/100g 52000-0419-80 Universal 337 g — — Discontinued —
Antibacterial Wipes .13 g/100g 71293-0020-01 ERC 2000 packets — — FDA listed —
Klean Freak .13 g/100g 78982-0001-01 KLEAN 4 g — — FDA listed —
Klean Freak .13 g/100g 78982-0003-01 KLEAN 4 g — — FDA listed —
Klean Freak .13 g/100g 78982-0006-01 KLEAN 4 g — — FDA listed —
Loris BZK Antiseptic Wipes .13 g/100g 68356-0126-01 LernaPharm 100 packets — — Discontinued —
McKesson Benzalkonium Chloride Towelette .13 g/100g 68599-5807-03 McKesson 100 packets — — FDA listed —
Zoviro .13 g/100g 83814-0004-01 Zoviro, 80 pouches — — FDA listed —
Antiseptic Towelettes .13 g/100g 49687-0011-01 CMC 10 patches — — FDA listed —
Zoom Wipes .13 g/100g 70401-0150-01 ZOOM 1500 packets — — Discontinued —
Antiseptic Wipe .13 g/100g 71584-0002-01 Guangdong 1.6 g — — FDA listed —
Safly BZK Antiseptic Towelette .13 g/100g 71734-0116-01 JIANGMEN 2 g — — FDA listed —
2XL Mega Rolls Sanitizing Wipes .13 g/100g 71995-0020-01 2xl 2300 packets — — FDA listed —
tazza JIM WIPES .13 g/100g 76370-0039-01 Tazza 1500 patches — — FDA listed —
tazza ECOFIT WIPES .13 g/100g 76370-0040-01 Tazza 1500 patches — — FDA listed —
Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent .13 g/100g 78691-0033-00 Quest 20 g — — FDA listed —
Klean Freak .13 g/100g 78982-0005-01 KLEAN 4 g — — FDA listed —
Klean Freak .13 g/100g 78982-0007-01 KLEAN 4 g — — FDA listed —
Sanitising Wipes .13 g/100g 81331-0001-13 Sportsmith, 800 nots — — Discontinued —
Wet Ones Antibacterial Hand Wipes Lavender Scent .13 g/100g 63354-0536-20 Edgewell 20 g — — FDA listed —
Diamond Wipes Antibacterial Hand Wipes .13 g/100g 64709-0111-10 Diamond 1 g — — FDA listed —
Antibacterial Wet wipes .13 g/100g 73760-0001-01 Zhejiang 15 pouches — — FDA listed —
tazza HAND SANITIZER KING WIPES .13 g/100g 76370-0030-01 Tazza 950 patches — — FDA listed —
MediChoice OB Cleansing .13 g/100g 39892-0306-01 O&M 1000 patches — — FDA listed —
McKesson Obstetrical Antiseptic Towelette .13 g/100g 68599-5806-03 McKesson 100 packets — — FDA listed —
Sanitizing Wipes .13 g/100g 70972-1200-01 Wipes 1200 packets — — FDA listed —
Antibacterial Bandages .13 g/100g 71584-0111-01 Guangdong 5 g — — FDA listed —
Simplify Antibacterial Hand Wipes .13 g/100g 11822-0286-02 RITE 24 patches — — FDA listed —
Antibacterial Hand wipes .13 g/100g 51628-9999-01 MY 12 g — — FDA listed —
Crayola ANTIBACTERIAL HAND WIPES .13 g/100g 70108-0310-01 ASHTEL 20 patches — — FDA listed —
Keep Going Non Sting Cleaning Wipe .13 g/100g 71734-0343-01 JIANGMEN 2 g — — FDA listed —
Go Home And Haven Antibacterial Hand Wipes .13 g/100g 85828-0301-01 Grocery 124 g — — FDA listed —
KeepGoing Non Sting Cleaning Wipe .13 g/100g 82942-1007-01 J&A 5 g — — FDA listed —
24 7 life by 7 Eleven Antibacterial HAND WIPES .13 g/100g 10202-0402-01 7-ELEVEN, 20 patches — — FDA listed —
Alta Antibacterial Hand Wipes .13 g/100g 79165-0777-20 Alta 1 packet — — FDA listed —
DrugStore Antibacterial Hand Wipes .13 g/100g 29485-6666-01 Lil' 30 patches — — 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

🏛️
2026
On the market since
Feb 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for BENZALKONIUM CHLORIDE — the ingredient across all brands.

Top reported reactions

Drug Hypersensitivity124
Arthralgia117
Condition Aggravated115
Pain In Extremity114
Infection111
Musculoskeletal Stiffness111
Joint Swelling109

Age at onset

Infant1
Child1
Adolescent3
Adult41
Elderly17

Reporter sex

479 reports
Male · 32%
Female · 68%
Unknown · 0%

Serious outcomes

Hospitalization211
Life-threatening33
Death31
Disabling23
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 81 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
83004-0033-01 You're viewing this 1 BOX in 1 CARTON (83004-033-01) / 120 g in 1 BOX 2026-02-04 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
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) ✓ 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.
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 83004-033-01, 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: 83004-0033-01, written without dashes as 83004003301. 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 83004-0033-01, the first segment (83004) is the labeler code FDA assigned to Rida LLC; the middle segment (0033) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Rida LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Rida LLC 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 24 words ▾

Uses For washing to reduce bacteria on the skin Helps cleanse and detoxify skin Aids in controlling body odor and breakouts caused by bacteria

⏱️ Dosage and Administration 20 words ▾

Directions Wet skin and bar Work into lather and apply to affected areas Rinse thoroughly Use daily or as needed

⚠️ Warnings 49 words ▾

Warnings For external use only. Avoid contact with the eyes . If contact occurs, rinse thoroughly with water. If irritation or redness develops , stop use and consult a physician. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately.

🧪 Active Ingredient 5 words ▾

Active ingredient Benzalkonium Chloride (0.13%)

🧪 Inactive Ingredients 50 words ▾

Inactive ingredients Sodium Palmate, Sodium Palm Kernelate, Aqua (Water), Glycerin, Charcoal Powder, Mel (Manuka Honey) Extract, Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea) Butter, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricaria) Flower Extract, Calendula Officinalis Flower Extract, Tocopheryl Acetate, Citric Acid, Fragrance, Sodium Chloride, Sodium Gluconate, Titanium Dioxide, Phenoxyethanol, Ethylhexylglycerin.

🎯 Purpose 2 words ▾

Purpose Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 83004-0032-01 · Rida 83004-0034-01 · Rida →
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.