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Escudo Ultra-Protect Soft Care Benzalkonium Chloride .1 g/100g Soap, 115 g

by Indelpa, Inc. · 115 g in 1 CELLO PACK (84529-002-01)
NDC 84529-0002-01
🏷️ FDA NDC (as labeled) 84529-002-01 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-0374-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 84529-002-01
Product NDC 84529-002
11-digit billing NDC 84529000201
RxCUI 1926450
UNII F5UM2KM3W7
Application # M003
SPL Set ID 1cc4b68b-dceb-3fab-e063-6294a90ab112
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-07-08
Route TOPICAL
Dosage form SOAP
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 84529-002-01 — 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 → 84529-0002-01. 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

LabelerIndelpa, Inc.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code84529
First marketedJul 2024
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?

Escudo Ultra-Protect Soft Care is a topical soap containing benzalkonium chloride, an antimicrobial agent. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rules for antiseptic soaps rather than undergoing individual product review. Benzalkonium chloride is commonly used in cleansing products for its antimicrobial properties. This soap is applied to the skin during bathing or handwashing.

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.
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
Dial refresh and renew Antibacterial Mountain Fresh .1 g/100g 54340-0017-03 Henkel 3 packets — — FDA listed —
Dial Antibacterial with Vitamins .1 g/100g 54340-0020-01 Henkel 113 g — — FDA listed —
Dial refresh and renew Antibacterial white .1 g/100g 54340-0260-01 Henkel 113 g — — FDA listed —
Dial advanced clean Antibacterial gold .1 g/100g 54340-0262-01 Henkel 113 g — — FDA listed —
Dial Antibacterial Calm and Soothe .1 g/100g 54340-0266-03 Henkel 3 packets — — FDA listed —
Dial Antibacterial and Sensitive Aloe .1 g/100g 54340-0267-03 Henkel 16 cellos — — FDA listed —
Dial Complete Antibacterial Bar Spring Water .1 g/100g 54340-0270-08 Henkel 8 packets — — FDA listed —
Dial Antibacterial Bar .1 g/100g 54340-0272-20 Henkel 99 g — — FDA listed —
Dial Antibacterial Bar .1 g/100g 54340-0274-01 Henkel 180 g — — Discontinued —
Dial Antibacterial Bar .1 g/100g 54340-0278-04 Henkel 678 g — — Discontinued —
Dial antibacterial and sensitive hypoallergenic bar .1 g/100g 54340-0283-30 Henkel 1 cello — — FDA listed —
Dial Antibacterial Vitamin Bar .1 g/100g 54340-0286-02 Henkel 72 cellos — — FDA listed —
Dial refresh and renew Antibacterial Bar Spring Water .1 g/100g 54340-0300-01 Henkel 113 g — — FDA listed —
DK12 Oatmeal Antibacterial and Moisturizing .1 g/110g 62476-0104-15 Industria 140 g — — FDA listed —
DK12 Creamy Antibacterial and Moisturizing .1 g/110g 62476-0105-15 Industria 140 g — — FDA listed —
DK12 Fresh Energy Antibacterial and Moisturizing .1 g/110g 62476-0106-15 Industria 140 g — — FDA listed —
Escudo Ultra-Protect Original .1 g/100g 84529-0001-01 Indelpa, 115 g — — FDA listed —
Escudo Ultra-Protect Soft Care .1 g/100gthis 84529-0002-01 Indelpa, 115 g — — FDA listed —
Gelle-N-Detox Ice Mint And Eucalyptus Massage .1 g/100g 49283-0014-07 CHEMCO 20 g — — Discontinued —
Gelle-N-Detox - Lavender And Rosemary Massage .1 g/100g 49283-0001-07 CHEMCO 20 g — — FDA listed —
Gelle-N-Detox Ice Mint And Eucalyptus Massage .1 g/100g 49283-0110-07 CHEMCO 20 g — — FDA listed —
Klean-Them Hand Sanitizing Towels .1 g/100g 73943-0953-01 Rite-Kem, 400 g — — FDA listed —
5EWA5 Antibacterial Hand Sanitizer Wipes .1 g/100g 40096-1909-01 W.W. 6 canisters — — Discontinued —
Gelle-N-Detox - Lavender And Rosemary Massage .1 g/100g 49283-0015-07 CHEMCO 20 g — — Discontinued —
SCRUBS Hand Sanitizer Wipes .1 g/100g 51239-2909-01 ITW 400 g — — 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
Jul 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
84529-0002-01 You're viewing this 115 g in 1 CELLO PACK (84529-002-01) 2024-07-09 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) — 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.
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 84529-002-01, 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: 84529-0002-01, written without dashes as 84529000201. 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 84529-0002-01, the first segment (84529) is the labeler code FDA assigned to Indelpa, Inc.; the middle segment (0002) 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 Indelpa, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Indelpa, 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 18 words ▾

Use For washing to decrease bacteria on the skin.

Uses for washing to decrease bacteria on the skin.

⏱️ Dosage and Administration 16 words ▾

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

⚠️ Warnings 89 words ▾

Warnings For external use only. Do not use Do not use if you are allergic to any of the ingredients. When using this product When using this product avoid contact with eyes.

In case of eye contact, rinse thoroughly with water. Stop use and ask a doctor Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours. Keep out of reach of children Keep out of reach of children.

If swallowed, get medical help or contact a Poisn Center right away.

🧪 Active Ingredient 28 words ▾

Active ingredient Active ingredient ------------------------- Purpose Benzalkonium Chloride 0.1% .......... Antibacterial Active ingredient -------------------------Purpose Benzalkonium Chloride 0.1% .......... Antibacterial Use For washing to decrease bacteria on the skin.

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients Alcohol, Benzyl Benzoate, Etidronic Acid, Glycerin, Sodium Chloride, Sodium Kernelate, Sodium Palmate, Tetrasodium EDTA, Titanium Dioxide, Water, Fragrance.

🎯 Purpose 17 words ▾

Active ingredient -------------------------Purpose Benzalkonium Chloride 0.1% .......... Antibacterial Use For washing to decrease bacteria on the skin.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84529-0001-01 · Indelpa, 84530-0100-04 · The →
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.