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FoamFresh Dye Free Antibacterial Hand Wash CHLOROXYLENOL 2.5 mg/mL Solution, 750 mL — NDC 11429-1010-07 package photo

FoamFresh Dye Free Antibacterial Hand Wash CHLOROXYLENOL 2.5 mg/mL Solution, 750 mL

by Woodbine Products Company · 750 mL in 1 BOTTLE, PLASTIC (11429-1010-7)
NDC 11429-1010-07
🏷️ FDA NDC (as labeled) 11429-1010-7 billing pads the package segment with a zero
This package
Contains750 mL Pack sizes4 compare ↓
Also comes in: 30 ml 11429-1010-01 1000 ml 11429-1010-03 1250 ml 11429-1010-08
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

Past resolved recalls for this product (1)
Class III · Aug 30, 2022 · Terminated — Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label. (Woodbine Products Co Inc) · FDA recall D-0006-2023

🆔 Identity & classification

FDA NDC (as labeled) 11429-1010-7
Product NDC 11429-1010
11-digit billing NDC 11429101007
RxCUI 1435989
UNII 0F32U78V2Q
Application # 505G(a)(3)
SPL Set ID ba205f78-6e3f-483e-a37a-537f6917b00c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-11-20
Route TOPICAL
Dosage form SOLUTION
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 11429-1010-7 — a 5-4-1 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 package segment → 11429-1010-07. 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 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

LabelerWoodbine Products Company
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code11429
First marketedNov 2018
Product typeHuman Otc Drug
Portfolio7 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?

FoamFresh Dye Free Antibacterial Hand Wash is a topical foam solution containing chloroxylenol, an antimicrobial ingredient. Chloroxylenol is commonly used in over-the-counter hand soaps and cleansers to help reduce bacteria on the skin. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for antibacterial hand wash products rather than having undergone individual FDA review. It is intended for routine handwashing to help maintain skin cleanliness.

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 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 Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • UNII BYR0546TOW
    DMDM hydantoin is a preservative chemical used to prevent the growth of bacteria and fungi in medicines. It helps keep the product safe and stable throughout its shelf life.
  • UNII 76LN7P7UCU
    Lauryl glucoside is a mild plant-based cleansing agent made from coconut oil and glucose. It's used in medicines as a surfactant to help dissolve and distribute ingredients evenly throughout the formulation.
  • 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 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.

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

The official label also statesInactive Ingredients: Water, Sodium Lauryl Sulfate, Lauryl Glucoside, Cocamidopropyl Betaine, Decyl Glucoside. Potassiom Hydrolyzed Collagen, DMDM Hydantoin, Propylene Glycol and Fragrance

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 mLPer 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: 30 ml 1000 ml 1250 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
FoamFresh Dye Free Antibacterial Hand Wash 2.5 mg/mLthis 11429-1010-07 Woodbine 750 ml — — FDA listed —
Asepso Antiseptic Original 2.5 mg/g 49698-0001-01 CODAA 80 g — — FDA listed —
Waxie Antibacterial Hand 2.5 g/L 61666-0901-23 Waxie's 47 l — — FDA listed —
Antibacterial Foam Hand Wash 2.5 mg/mL 63039-1005-03 Chemco 1000 ml — — FDA listed —
Meringue Foaming Dye Free Antibacterial 2.5 mg/mL 63998-0758-01 United 750 ml — — FDA listed —
FoamFresh Antibacterial Hand Wash 2.5 mg/mL 11429-1005-00 Woodbine 1125 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

🏛️
2018
On the market since
Nov 2018
📍
2026
Currently FDA-listed
8 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
11429-1010-01 30 mL in 1 BOTTLE, PLASTIC (11429-1010-1) 2018-11-20 Active
11429-1010-03 1000 mL in 1 BOTTLE, PLASTIC (11429-1010-3) 2018-11-20 Active
11429-1010-07 You're viewing this 750 mL in 1 BOTTLE, PLASTIC (11429-1010-7) 2018-11-20 Active
11429-1010-08 1250 mL in 1 BOTTLE, PLASTIC (11429-1010-8) 2018-11-20 Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 11429-1010-07?
NDC 11429-1010-07 contains 750 mL — 750 ml in 1 bottle, plastic.
What is the difference between NDC 11429-1010-07 and NDC 11429-1010-01?
Both are FoamFresh Dye Free Antibacterial Hand Wash CHLOROXYLENOL 2.5 mg/mL Solution — the drug itself is identical. NDC 11429-1010-07 is the 750 mL package, while NDC 11429-1010-01 is the 30 ml package.
What NDC number is used to bill for this package of FoamFresh Dye Free Antibacterial Hand Wash CHLOROXYLENOL 2.5 mg/mL Solution?
Bill NDC 11429-1010-07 — the 11-digit billing format is 11429101007. 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
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 FDA registers it as 11429-1010-7, 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: 11429-1010-07, written without dashes as 11429101007. 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 11429-1010-07, the first segment (11429) is the labeler code FDA assigned to Woodbine Products Company; the middle segment (1010) 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.
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 Woodbine Products 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 3 other package presentations of this same product, including 30 ml (11429-1010-01), 1000 ml (11429-1010-03), 1250 ml (11429-1010-08). 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?
Woodbine Products 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.

📄 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 10 words ▾

Uses: For hand washing to decrease bacteria on the skin.

⏱️ Dosage and Administration 17 words ▾

Directions: For maximum efficiency, pump foam into dry hands, lather vigorous for 30 seconds, rinse and dry.

⚠️ Warnings 70 words ▾

Warnings: For external use only When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children. Children must be supervised in use of this product. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 9 words ▾

Other Information: Store at 20 to 25C.(68 to 77F)

🧪 Active Ingredient 4 words ▾

Active Ingredient Chloroxylenol 0.25%

🧪 Inactive Ingredients 21 words ▾

Inactive Ingredients: Water, Sodium Lauryl Sulfate, Lauryl Glucoside, Cocamidopropyl Betaine, Decyl Glucoside. Potassiom Hydrolyzed Collagen, DMDM Hydantoin, Propylene Glycol and Fragrance

🎯 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 ↗
← 11429-1006-01 · Woodbine 11489-0182-01 · BCM →
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.