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Protex Complete Antibacterial Bar Chloroxylenol 3 mg/g Soap — NDC 35000-0069-06 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Protex Complete Antibacterial Bar Chloroxylenol 3 mg/g Soap — NDC 35000-069-06 (Billing 35000-0069-06)

by Colgate-Palmolive Company · 6 CARTON in 1 CELLO PACK / 1 APPLICATOR in 1 CARTON / 104.8 g in 1 APPLICATOR

This is a package of Protex Complete Antibacterial Bar Chloroxylenol 3 mg/g Soap from Colgate-Palmolive Company, marketed since Dec 2021 and currently FDA-listed.

NDC 35000-0069-06
🏷️ FDA NDC (as labeled) 35000-069-06 billing pads the product segment with a zero
This package
Contains104.8 g in 1 applicator Pack sizes3 compare ↓
Product page 35000-0069-01 Also comes in: 104.8 g 35000-069-01 104.8 g 35000-069-03
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 35000-069-06 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
35000 labeler · 069 product · 06 package
Package marketed since
Dec 1, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 3500006906 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 35000-069-06
Product NDC 35000-069
11-digit billing NDC 35000006906
RxCUI 1860597
UNII 0F32U78V2Q
Application # 505G(a)(3)
SPL Set ID 8ce05d5c-f710-463d-b15f-160791f791ae
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-12-01
Route TOPICAL
Dosage form SOAP
Substance CHLOROXYLENOL
Quick answers
  • RxCUI (RxNorm): 1860597
Why two NDCs? The FDA registers this code as 35000-069-06 — 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 → 35000-0069-06. 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 Phenol and derivatives class.

Drug family (ATC) Phenol and derivatives
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.

Clinical

🧪 What is this product?

Protex Complete Antibacterial Bar is a bar soap containing chloroxylenol, an antimicrobial ingredient. Chloroxylenol is typically used in over-the-counter cleansing products to help reduce bacteria on the skin. This is an OTC monograph drug, meaning it is marketed under FDA's established rules for antibacterial soaps rather than as an individually reviewed product. The soap is applied topically during routine handwashing and bathing.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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: 104.8 g 104.8 g
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
35000-0069-01 35000-069-01 Main listing 1 APPLICATOR in 1 CARTON / 104.8 g in 1 APPLICATOR 2021-12-01 — Active
35000-0069-03 35000-069-03 3 CARTON in 1 CELLO PACK / 1 APPLICATOR in 1 CARTON / 104.8 g in 1 APPLICATOR 2021-12-01 — Active
35000-0069-06 You're viewing this 6 CARTON in 1 CELLO PACK / 1 APPLICATOR in 1 CARTON / 104.8 g in 1 APPLICATOR 2021-12-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 6 carton in 1 cello pack / 1 applicator in 1 carton / 104.8 g in 1 applicator.
What NDC number is used to bill for this package of Protex Complete Antibacterial Bar Chloroxylenol 3 mg/g Soap?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Protex Complete Antibacterial Bar 3 mg/gthis 35000-0069-06 Colgate-Palmolive 1 cello — — FDA listed —
Ban-Aid 3 mg/mL 63830-0544-06 Pro 800 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

🏛️
2021
On the market since
Dec 2021
📍
2026
Currently FDA-listed
5 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.

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 MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
  • UNII M2F465ROXU
    A phosphorus-containing compound used as a chelating agent and water softener in pharmaceutical formulations. It helps prevent mineral buildup and stabilizes the medicine by binding to metal ions that could otherwise degrade the product.
  • 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 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 K146MR5EXO
    Sodium laurate is a salt derived from lauric acid, a natural fatty acid. It works as an emulsifier and surfactant to help mix oil and water-based ingredients together in the medicine.
  • UNII 872C9A1W9I
    Sodium linoleate is a salt derived from linoleic acid, a plant-based fatty acid. It functions as an emulsifier and solubilizer, helping to mix oil and water-based ingredients together in liquid formulations.
  • UNII 399SL044HN
    Sodium oleate is a salt derived from oleic acid, a natural fatty acid. In medicines, it acts as an emulsifier and surfactant, helping mix oil and water ingredients together and improving how the drug dissolves and spreads in the body.
  • UNII JQ43KP6296
    Sodium palmitate is a salt derived from palmitic acid, a naturally occurring fatty acid. It acts as an emulsifier and surfactant in medicines, helping mix oil and water-based ingredients and improving product stability and texture.
  • 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.

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

The official label also statesSodium Laurate/Linoleate/Oleate/Palmitate, Water, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Etidronic Acid, Titanium Dioxide.

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.

Manufacturer & labeler

LabelerColgate-Palmolive Company
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code35000
First marketedDec 2021
Product typeHuman Otc Drug
Portfolio190 products on file

More NDCs from Colgate-Palmolive Company labeler code 35000

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.

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 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Use Helps reduce bacteria that potentially can cause disease

⏱️ Dosage and Administration 13 words ▾

Directions Wet bar with water. Lather and wash skin. Rinse and dry thoroughly.

⚠️ Warnings 43 words ▾

Warnings For external use only. When using this product, avoid contact with eyes. In case of contact, flush with water. Keep out of reach of children, except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 4 words ▾

Active ingredient Chloroxylenol 0.30%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Sodium Laurate/Linoleate/Oleate/Palmitate, Water, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Etidronic Acid, Titanium Dioxide.

🎯 Purpose 2 words ▾

Purpose Antibacterial

📄 When Using This Product 15 words ▾

When using this product, avoid contact with eyes. In case of contact, flush with water.

📄 Keep Out of Reach of Children 23 words ▾

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

📄 Questions or Comments 2 words ▾

Questions? 1-800-443-0602

📄 Package Label / Principal Display Panel 41 words ▾

PRINCIPAL DISPLAY PANEL - 104.8 g Applicator Carton NEW Eliminates 99.9% of bacteria* Protex ® For the Good Health of your Skin COMPLETE Antibacterial Antibacterial Bar Soap NET WT

3.7OZ (104.8 g) PRINCIPAL DISPLAY PANEL - 104.8 g Applicator Carton

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 ✓ Available
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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Colgate-Palmolive Company. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 1 applicator (35000-0069-01), 1 cello (35000-0069-03). 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?
Colgate-Palmolive Company 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.
← 35000-0066-41 · Colgate-Palmolive 35000-0070-81 · Colgate-Palmolive →
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.