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Osceola Supply Inc 6176 CHLOROXYLENOL 6 mg/mL Soap, 1200 mL — NDC 62672-0300-01 package photo

Osceola Supply Inc 6176 CHLOROXYLENOL 6 mg/mL Soap, 1200 mL

by OSCEOLA SUPPLY, INC. · 1200 mL in 1 CARTRIDGE (62672-300-01)
NDC 62672-0300-01
🏷️ FDA NDC (as labeled) 62672-300-01 billing pads the product segment with a zero
This package
Contains1200 mL Pack sizes21 compare ↓
Also comes in: 50 ml 62672-0300-18 118 ml 62672-0300-24 149 ml 62672-0300-28 236 ml 62672-0300-16 350 ml 62672-0300-03 532 ml 62672-0300-17 540 ml 62672-0300-05 700 ml 62672-0300-07 800 ml 62672-0300-13 800 ml 62672-0300-27 946 ml 62672-0300-15 1000 ml 62672-0300-10 1000 ml 62672-0300-11 1000 ml 62672-0300-12 1325 ml 62672-0300-35 1890 ml 62672-0300-19 2000 ml 62672-0300-09 2082 ml 62672-0300-55 3785 ml 62672-0300-14 7560 ml 62672-0300-20
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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. 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) 62672-300-01
Product NDC 62672-300
11-digit billing NDC 62672030001
RxCUI 413262
UNII 0F32U78V2Q
Application # M003
SPL Set ID a7dcc6b1-655d-41b3-ab97-913bc4aae01f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2016-07-22
Route TOPICAL
Dosage form SOAP
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 62672-300-01 — 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 → 62672-0300-01. 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 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.

🏭 Manufacturer & labeler

LabelerOSCEOLA SUPPLY, INC.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code62672
First marketedJul 2016
Product typeHuman Otc Drug
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 topical soap containing chloroxylenol, an antimicrobial agent commonly used in hand and body cleansing products. Chloroxylenol is typically added to soaps to help reduce bacteria on the skin during washing. This product is marketed as an OTC monograph drug, meaning it is made according to FDA's established rules for antimicrobial soaps rather than as an individually approved drug application.

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.

🧪 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII R57ZHV85D4
    Boric acid is a weak acid derived from boron. In medicines, it typically serves as a buffer to help maintain the product's pH level and may act as a preservative in certain formulations.
  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII 09179OX7TB
    PEG-75 Lanolin is a waxy substance derived from sheep's wool that has been chemically modified to mix easily with water and oil. It acts as an emulsifier and moisturizer in topical formulations, helping blend different ingredients and soften the skin.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • 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 BPV390UAP0
    Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
  • UNII 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • 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.

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

The official label also stateswater, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, propylene glycol, sodium chloride, PEG-75 lanolin, sodium styrene/PEG-10 maleate/nonoxynol-10 maleate/acrylates copolymer, boric acid, fragrance, methylparaben, propylparaben, aloe barbadensis

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.
Try another pack size: 50 ml 118 ml 149 ml 236 ml 350 ml 532 ml 540 ml 700 ml 800 ml 800 ml 946 ml 1000 ml 1000 ml 1000 ml 1325 ml 1890 ml 2000 ml 2082 ml 3785 ml 7560 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
Antibacterial 6.046 g/L 00404-4441-01 Henry 55 l — — FDA listed —
Saniwash Antimicrobial Foaming Hand .006 g/mL 61010-8600-01 Safetec 550 ml — — FDA listed —
Osceola Supply Inc 6176 6 mg/mLthis 62672-0300-01 OSCEOLA 1200 ml — — Discontinued —
Servo-Stat P .6 g/100mL 76378-0017-01 Enzyme 50 ml — — FDA listed —
Servo-Stat P Antiseptic Hand Wash .6 g/100mL 76378-0021-01 Enzyme 118 ml — — FDA listed —
Servo-Stat P Foam Antiseptic Hand Wash .6 g/100mL 76378-0022-01 Enzyme 473 ml — — FDA listed —
Micro-Aseptic .6 g/100mL 81591-0001-01 ASEPTIC 118 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

🏛️
2016
On the market since
Jul 2016
📍
2026
Currently FDA-listed
10 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
62672-0300-01 You're viewing this 1200 mL in 1 CARTRIDGE (62672-300-01) 2016-07-22 Discontinued by firm
62672-0300-03 350 mL in 1 CARTRIDGE (62672-300-03) 2016-07-22 Discontinued by firm
62672-0300-05 540 mL in 1 BOTTLE, PLASTIC (62672-300-05) 2016-07-22 Discontinued by firm
62672-0300-07 700 mL in 1 BAG (62672-300-07) 2016-07-22 Discontinued by firm
62672-0300-09 2000 mL in 1 CARTRIDGE (62672-300-09) 2016-07-22 Discontinued by firm
62672-0300-10 1000 mL in 1 CARTRIDGE (62672-300-10) 2016-07-22 Discontinued by firm
62672-0300-11 1000 mL in 1 BOTTLE, PLASTIC (62672-300-11) 2016-07-22 Discontinued by firm
62672-0300-12 1000 mL in 1 BAG (62672-300-12) 2016-07-22 Active
62672-0300-13 800 mL in 1 BAG (62672-300-13) 2016-07-22 Active
62672-0300-14 3785 mL in 1 BOTTLE, PLASTIC (62672-300-14) 2016-07-22 Active
62672-0300-15 946 mL in 1 BOTTLE, PLASTIC (62672-300-15) 2016-07-22 Active
62672-0300-16 236 mL in 1 BOTTLE, PLASTIC (62672-300-16) 2016-07-22 Discontinued by firm
62672-0300-17 532 mL in 1 BOTTLE, PLASTIC (62672-300-17) 2016-07-22 Active
62672-0300-18 50 mL in 1 BOTTLE, PLASTIC (62672-300-18) 2016-07-22 Discontinued by firm
62672-0300-19 1890 mL in 1 CONTAINER (62672-300-19) 2016-07-22 Discontinued by firm
62672-0300-20 7560 mL in 1 DRUM (62672-300-20) 2016-07-22 Discontinued by firm
62672-0300-24 118 mL in 1 BOTTLE, PLASTIC (62672-300-24) 2016-07-22 Discontinued by firm
62672-0300-27 800 mL in 1 CARTRIDGE (62672-300-27) 2016-07-22 Discontinued by firm
62672-0300-28 149 mL in 1 BOTTLE, PLASTIC (62672-300-28) 2016-07-22 Discontinued by firm
62672-0300-35 1325 mL in 1 DRUM (62672-300-35) 2016-07-22 Discontinued by firm
62672-0300-55 2082 mL in 1 DRUM (62672-300-55) 2016-07-22 Discontinued by firm

Pack size FAQ

What quantity is in NDC 62672-0300-01?
NDC 62672-0300-01 contains 1200 mL — 1200 ml in 1 cartridge.
What is the difference between NDC 62672-0300-01 and NDC 62672-0300-18?
Both are Osceola Supply Inc 6176 CHLOROXYLENOL 6 mg/mL Soap — the drug itself is identical. NDC 62672-0300-01 is the 1200 mL package, while NDC 62672-0300-18 is the 50 ml package.
What NDC number is used to bill for this package of Osceola Supply Inc 6176 CHLOROXYLENOL 6 mg/mL Soap?
Bill NDC 62672-0300-01 — the 11-digit billing format is 62672030001. 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 ✓ 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.
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 62672-300-01, 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: 62672-0300-01, written without dashes as 62672030001. 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 62672-0300-01, the first segment (62672) is the labeler code FDA assigned to OSCEOLA SUPPLY, INC.; the middle segment (0300) 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 20 other package presentations of this same product, including 50 ml (62672-0300-18), 118 ml (62672-0300-24), 149 ml (62672-0300-28). 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?
OSCEOLA SUPPLY, 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 15 words ▾

Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin

⏱️ Dosage and Administration 28 words ▾

Drug Facts Box OTC-Dosage & Administration Section wet hands and forearms apply 5 milliliters (teaspoonful) or palmful to hands and forearms scrub thoroughly for 1 minute and rinse

⚠️ Warnings 9 words ▾

Drug Facts Box OTC-Warnings Section For external use only

🧪 Active Ingredient 8 words ▾

Drug Facts Box OTC-Active Ingredient Section Chloroxylenol 0.6%

🧪 Inactive Ingredients 33 words ▾

Drug Facts Box OTC-Inactive Ingredient Section water, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, propylene glycol, sodium chloride, PEG-75 lanolin, sodium styrene/PEG-10 maleate/nonoxynol-10 maleate/acrylates copolymer, boric acid, fragrance, methylparaben, propylparaben, aloe barbadensis

🎯 Purpose 6 words ▾

Drug Facts Box OTC-Purpose Section Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 62671-0001-01 · Vantage 62673-0017-94 · Neoteric →
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.