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TOUCH Sanitizing Germ Block, Mint Green Tea Aloe, 1oz (28.35g) benzalkonium chloride .13 g/100g Aerosol, Spray, 43 g — NDC 69744-0202-01 package photo

TOUCH Sanitizing Germ Block, Mint Green Tea Aloe, 1oz (28.35g) benzalkonium chloride .13 g/100g Aerosol, Spray, 43 g

by Relevo, Inc. · 43 g in 1 BOTTLE, SPRAY (69744-0202-1)
NDC 69744-0202-01
🏷️ FDA NDC (as labeled) 69744-0202-1 billing pads the package 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-0360-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 69744-0202-1
Product NDC 69744-0202
11-digit billing NDC 69744020201
RxCUI 1039012
UNII F5UM2KM3W7
UPC 0862622000130, 0862622000116, 0862622000109, 0862622000123
Application # part333A
SPL Set ID c3ba1f21-51d9-c4ee-e053-2995a90aa042
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH NOT FINAL
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-05-07
Marketing end 2027-05-01
Route TOPICAL
Dosage form AEROSOL, SPRAY
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 69744-0202-1 — 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 → 69744-0202-01. 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

LabelerRelevo, Inc.
FDA applicationpart333A (OTC MONOGRAPH NOT FINAL)
Labeler code69744
First marketedMay 2021
Product typeHuman Otc Drug
Portfolio4 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?

This is a topical antiseptic spray marketed as an over-the-counter antimicrobial sanitizer under the OTC monograph category. The active ingredient, benzalkonium chloride, is an antimicrobial agent typically used in hand sanitizers and surface disinfectants to reduce germs on skin and surfaces. The product is supplied as an aerosol spray in a 1-ounce container and is intended for topical application. The formulation also contains mint, green tea, and aloe, which are common botanical additives in sanitizing products.

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.

💊 What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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.

  • 95 g / 100 g UNII NMQ347994Z
    Cyclomethicone is a silicone-based fluid that acts as a lubricant and solvent in medicines. It helps products flow smoothly, reduces friction between particles, and aids in even distribution of active ingredients.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesInactive Ingredients • Cyclopentasiloxane, Dimethyl Ether, Alcohol Denat, Prunus Amygdalus Dulcis (Sweet Almond Oil), Butyrospermum Parkii (Shea) Butter, Fragrance, Methyl Dihydrojasmonate

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.
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
Wound Wash Antiseptic Saline with Benzalkonium Chloride 1.3 mg/mL 13709-0235-11 NeilMed 75 ml — — FDA listed —
X3 Clean 1.3 mg/mL 26550-0002-10 X3 8 ml — — FDA listed —
Lightning X Antiseptic 1.3 mg/100mL 43473-0303-01 Nantong 59.1 ml — — FDA listed —
Antiseptic 1.3 g/L 47682-0245-02 Unifirst 0591 l — — FDA listed —
Medi-First Antiseptic 1.3 g/L 47682-0254-02 Unifirst 0591 l — — FDA listed —
Antiseptic 1.3 g/L 47682-0316-02 Unifirst 0591 l — — FDA listed —
Green Guard Antiseptic 1.3 g/L 47682-0317-02 Unifirst 0591 l — — FDA listed —
Green Guard Antiseptic 1.3 g/L 47682-0333-02 Unifirst 0591 l — — FDA listed —
American Red Cross Antiseptic Cleansing 1.3 mg/mL 51628-0035-01 MY 177 ml — — FDA listed —
American Red Cross Antiseptic Cleansing .13 g/100mL 51628-4440-01 MY 177 ml — — FDA listed —
GenRx Hand Sanitizing 1.3 mg/mL 59088-0315-16 PureTek 237 ml — — FDA listed —
DiaSinc 1.3 mg/mL 59088-0596-16 PureTek 237 ml — — FDA listed —
First Aid Antiseptic .13 g/100mL 59898-0401-10 Water-Jel 59 ml — — FDA listed —
X3 Clean Hand Sanitizer 1.3 mg/mL 66902-0038-02 Natural 59 ml — — FDA listed —
Zoono Wound Cleanser .13 g/100mL 69221-0204-01 Zoono 50 ml — — FDA listed —
Antiseptic 1.3 g/L 69396-0153-02 Trifecta 0591 l — — FDA listed —
TOUCH Sanitizing Germ Block, Unscented, 1oz (28.35g) .13 g/100g 69744-0201-01 Relevo, 43 g — — FDA listed —
TOUCH Sanitizing Germ Block, Mint Green Tea Aloe, 1oz (28.35g) .13 g/100gthis 69744-0202-01 Relevo, 43 g — — FDA listed —
TOUCH Sanitizing Germ Block, Tropical Breeze, 1oz (28.35g) .13 g/100g 69744-0203-01 Relevo, 43 g — — FDA listed —
TOUCH Sanitizing Germ Block, Ocean Mist, 1oz (28.35g) .13 g/100g 69744-0204-01 Relevo, 43 g — — FDA listed —
ECOLAB Antiseptic 1.3 g/L 71338-0122-02 ECOLAB 059 l — — FDA listed —
My-Shield Hand Sanitizer .13 g/100mL 71884-0012-00 Enviro 10 ml — — FDA listed —
Germfree24 Hand Sanitizer .13 g/100mL 71884-0016-01 Enviro 10 ml — — FDA listed —
FIRST SHIELD First Aid Antiseptic .13 g/100mL 72976-0003-01 Ever 60 ml — — FDA listed —
American Red Cross Antiseptic Cleansing .13 g/100mL 75742-0037-01 Zhejiang 177 ml — — FDA listed —
MEDI-FIRST First Aid Antiseptic 1.3 mg/mL 78495-0122-01 Ultra 59.1 ml — — FDA listed —
Snugell .13 g/100mL 80671-0005-33 QUANZHOU 473 ml — — Discontinued —
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
May 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
69744-0202-01 You're viewing this 43 g in 1 BOTTLE, SPRAY (69744-0202-1) 2021-05-07 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 ✓ 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 Not Final". 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 69744-0202-1, 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: 69744-0202-01, written without dashes as 69744020201. 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 69744-0202-01, the first segment (69744) is the labeler code FDA assigned to Relevo, Inc.; the middle segment (0202) 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 it is currently marketed — but Relevo, Inc. has reported a marketing end date of 2027-05-01, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
Relevo, 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 📋 Description
🎯 Indications and Usage 35 words ▾

Use • To eliminate bacteria and viruses on the skin that could cause disease. • Recommended for repeated use. • Use on any surface to decrease the spread of germs.† • 60 sprays per container.

⏱️ Dosage and Administration 30 words ▾

Dosage is based on total benzalkonium chloride (the API) concentration of 0.13%. A 2 second spray yields 300 mg of product which contains 0.39 mg of API on the hands.

⚠️ Warnings 66 words ▾

Warnings • For external use only - hands and any surface. When using this product • Keep out of eyes. In the case of contact with eyes, flush thoroughly with water. • Do not inhale or ingest. • Avoid contact with broken skin. Stop using and ask doctor if skin irritation develops. Keep out of reach of children. In case of accidental ingestion, seek professional assistance.

🧪 Active Ingredient 7 words ▾

Active Ingredients Purpose Benzalkonium chloride 0.13% Microbicide

🧪 Inactive Ingredients 21 words ▾

Inactive Ingredients • Cyclopentasiloxane, Dimethyl Ether, Alcohol Denat, Prunus Amygdalus Dulcis (Sweet Almond Oil), Butyrospermum Parkii (Shea) Butter, Fragrance, Methyl Dihydrojasmonate

🎯 Purpose 18 words ▾

The purpose of TOUCH Hand Sanitizer is to decrease the level of disease causing germs on the hands.

📋 Description 70 words ▾

TOUCH is a unique hand and surface sanitizing mist clinically proven to kill 99.99% of harmful germs. The active ingredient is a broad spectrum microbicide that helps prevent infection while decreasing illness causing germs for up to 6 hours! When applied you will experience the germ killing action while softening your hands. Patent Pending. Made in the USA. Manufactured by: REVELO LABS, LLC 510 W. Carmel Dr. Carmel, IN 46033

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 69744-0201-01 · Relevo, 69744-0203-01 · Relevo, →
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.