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germfree24 Sanitizing Body-Spray Benzalkonium Chloride .1 g/100mL Spray, 200 mL — NDC 71884-0017-07 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

germfree24 Sanitizing Body-Spray Benzalkonium Chloride .1 g/100mL Spray, 200 mL — NDC 71884-017-07 (Billing 71884-0017-07)

by Enviro Specialty Chemicals Inc · 200 mL in 1 BOTTLE, SPRAY

This is a package of 200 mL of germfree24 Sanitizing Body-Spray Benzalkonium Chloride .1 g/100mL Spray from Enviro Specialty Chemicals Inc, no longer marketed (first marketed Dec 2020), no longer in the FDA NDC Directory.

NDC 71884-0017-07
🏷️ FDA NDC (as labeled) 71884-017-07 billing pads the product segment with a zero
This package
Contains200 mL Pack sizes6 compare ↓
Product page 71884-0017-01 Also comes in: 10 ml 71884-017-01 50 ml 71884-017-03 57 ml 71884-017-02 473 ml 71884-017-16 3785 ml 71884-017-04
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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 71884-017-07 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
71884 labeler · 017 product · 07 package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0810076762128
FDA record last changed
Jul 24, 2026
⚠️
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 ↗
⚠️
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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 71884-017-07
Product NDC 71884-017
11-digit billing NDC 71884001707
RxCUI 1052947
UNII F5UM2KM3W7
UPC 0810076762128
Application # 505G(a)(3)
SPL Set ID 9099b7d6-b3af-43ad-922f-e6586c89addc
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2020-12-16
Route TOPICAL
Dosage form SPRAY
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1052947
Why two NDCs? The FDA registers this code as 71884-017-07 — 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 → 71884-0017-07. 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 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.

Clinical

🧪 What is this product?

Germfree24 Sanitizing Body-Spray is a topical spray containing benzalkonium chloride, an over-the-counter antimicrobial agent. This product is marketed under FDA's OTC monograph rules for antiseptic and antimicrobial sprays. Benzalkonium chloride is typically used as a skin antiseptic and disinfectant to help reduce bacteria on the skin surface. The spray form allows for easy application to exposed skin areas.

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 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: 10 ml 50 ml 57 ml 473 ml 3785 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
71884-0017-01 71884-017-01 Main listing 10 mL in 1 BOTTLE, SPRAY 2020-12-16 — Discontinued by firm
71884-0017-02 71884-017-02 57 mL in 1 BOTTLE, SPRAY 2020-12-16 — Discontinued by firm
71884-0017-04 71884-017-04 3785 mL in 1 BOTTLE, SPRAY 2020-12-16 — Active
71884-0017-07 You're viewing this 200 mL in 1 BOTTLE, SPRAY 2020-12-16 — Discontinued by firm
71884-0017-16 71884-017-16 473 mL in 1 BOTTLE, SPRAY 2020-12-16 — Active
71884-0017-03 71884-017-03 50 mL in 1 BOTTLE, SPRAY 2026-02-25 — Active

You're viewing one of 6 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 200 mL — 200 ml in 1 bottle, spray.
How does this package differ from NDC 71884-0017-01?
Both are germfree24 Sanitizing Body-Spray Benzalkonium Chloride .1 g/100mL Spray — the drug itself is identical. This page's package is the 200 mL one, while NDC 71884-0017-01 is the 10 ml package.
What NDC number is used to bill for this package of germfree24 Sanitizing Body-Spray Benzalkonium Chloride .1 g/100mL Spray?
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
My-Shield Sanitizing Body .1 g/100mL 71884-0009-02 Enviro 58 ml — — Discontinued —
germfree24 Sanitizing Body-Spray .1 g/100mLthis 71884-0017-07 Enviro 200 ml — — Discontinued —
Triple Shield .1 g/100mL 71884-0034-16 Enviro 473 ml — — Discontinued —
DOCTOR INKS Sanitizing BODY 1 mg/mL 71884-0202-01 Enviro 50 ml — — FDA listed —
Sipa hand sanitizer S.pray with Moisturizers .1 g/100mL 83502-0003-01 Tourel 50 ml — — FDA listed —
Hand Sanitizer .1 g/100mL 77238-0241-11 DGH 30 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

🏛️
2020
On the market since
Dec 2020
📍
2026
Currently FDA-listed
6 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 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 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 P4OYN7A2O9
    Deceth-6 is a synthetic surfactant derived from decyl alcohol. It helps other ingredients mix together and improves how the medication dissolves or spreads in the body.
  • 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 XGN40YQC7B
    A silicone-based compound that serves as a conditioning and anti-static agent in solid oral medications. It helps reduce friction between tablet surfaces and equipment during manufacturing and packaging.
  • 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.

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

The official label also statesAloe Barbadensis leaf extract, Agua, Citric Acid, Deceth-6, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

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

LabelerEnviro Specialty Chemicals Inc
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code71884
First marketedDec 2020
Product typeHuman Otc Drug
Portfolio22 products on file

More NDCs from Enviro Specialty Chemicals Inc labeler code 71884

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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses: First aid anti-microbial - Topical body sanitizer • Preventive antiseptic

⏱️ Dosage and Administration 19 words ▾

Directions: spray liberally over the entire body recommended for regular repeat application, product safe on all surfaces & fabric's.

⚠️ Warnings 60 words ▾

Warnings: Do not freeze. For external use only. Do not use in ears, eyes or mouth. • When using this product, avoid contact with the eyes. In case of contact, flush eyes with water. • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours. • Keep out of reach of children.

🧪 Active Ingredient 5 words ▾

Active Ingredient: Benzalkonium Chloride 0.10%

🧪 Inactive Ingredients 14 words ▾

Inactive Ingredients: Aloe Barbadensis leaf extract, Agua, Citric Acid, Deceth-6, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Keep Out of Reach of Children 7 words ▾

• Keep out of reach of children.

📄 Questions or Comments 6 words ▾

Questions? +1(888) 331-8332, Mon-Fri 9:00AM-5:00PM (EST)

📄 Package Label / Principal Display Panel 2 words ▾

Packaging SanitizingBodySpray

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 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 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 5 other package presentations of this same product, including 10 ml (71884-0017-01), 50 ml (71884-0017-03), 57 ml (71884-0017-02). 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?
Enviro Specialty Chemicals 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.
← 71884-0016-01 · Enviro 71884-0025-01 · Enviro →
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.