NDC 72033-0172-00 — Touchland Hydrating Hand Sanitizer Mist ALCOHOL Kit

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72033-172-00

Product NDC 72033-172

11-digit billing NDC 72033017200

RxCUI 1041849

UPC 0850071283907

Application # 505G(a)(3)

SPL Set ID d4eedb24-f7d2-4992-b822-f7ec45759c8d

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status Discontinued

FDA listing status Discontinued by firm (certified through Sep 2026)

Marketing start 2026-08-22

Dosage form KIT

Quick answers

RxCUI (RxNorm): 1041849

Why two NDCs? The FDA registers this code as 72033-172-00 — 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 → 72033-0172-00. 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.

FDA openFDA NDC Directory · synced Oct 1, 2026
FDA label on DailyMed · label index refreshed Oct 3, 2026
RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
Medi-Span GPI (licensed)
First Databank (licensed) · refreshed Oct 1, 2026

RxNorm drug class

This medicine belongs to the Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants, Antidotes, Nerve depressants

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.

RxClass (NLM) · catalog refreshed Oct 1, 2026

Clinical

📗 Our plain-language guide HelloPharmacist

It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...

📖 Read our full Alcohol guide →

Patient education

📘 MedlinePlus patient leaflet ↗

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.

MedlinePlus (NLM) · refreshed Oct 1, 2026
FDA label on DailyMed · label index refreshed Oct 3, 2026

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 system	Per each	Per 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.

CMS NADAC weekly file
CMS ASP pricing files · refreshed Sep 20, 2026
CMS Medicaid State Drug Utilization Data · refreshed Oct 4, 2026
CMS Part D plan pricing files · refreshed Sep 24, 2026
VA National Acquisition Center price file

Packaging — all sizes for this product

Package NDC	Description	Marketing start	Marketing end	Status
72033-0172-00 You're viewing this Main listing	1 KIT in 1 BOX / 1 KIT in 1 KIT * 30 mL in 1 BOTTLE, SPRAY * 30 mL in 1 BOTTLE, SPRAY * 30 mL in 1 BOTTLE, SPRAY * 30 mL in 1 BOTTLE, SPRAY	2026-08-22	—	Discontinued by firm

Therapeutic equivalents

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Northside Hospital Amenity Kit--GI Dept 59448-0201-00	ASP	1 kit	—	—	FDA listed	—
Touchland Power Mist Hydrating Hand Sanitizer 72033-0118-00	TOUCHLAND	1 kit	—	—	FDA listed	—
Alcohol 84956-0013-01	Dongguan	1 kit	—	—	FDA listed	—
Touchland Hydrating Hand Sanitizer Mistthis 72033-0172-00	Touchland	1 kit	—	—	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.

FDA openFDA NDC Directory · synced Oct 1, 2026
FDA Orange Book · refreshed Oct 3, 2026
CMS NADAC weekly file

Availability & generic status

🏛️

2026

On the market since

Aug 2026

📍

2026

Currently FDA-listed

listed with the FDA

🔒

·

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.

FDA Orange Book · refreshed Oct 3, 2026

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.

FDA label on DailyMed · label index refreshed Oct 3, 2026
FDA openFDA NDC Directory · synced Oct 1, 2026

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

LabelerTouchland LLC

FDA application505G(a)(3) (OTC MONOGRAPH DRUG)

Labeler code72033

First marketedAug 2026

Product typeHuman Otc Drug

Portfolio41 products on file

More NDCs from Touchland LLC labeler code 72033

🔎 All NDCs from Touchland LLC

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 openFDA NDC Directory · synced Oct 1, 2026
Drugs@FDA

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel

🎯 Indications and Usage 52 words ▾

Uses Hand sanitizer to decrease bacteria on the skin. Recommended for repeated use.

⏱️ Dosage and Administration 140 words ▾

Directions spray enough product in your palm to thoroughly cover your hands. rub hands together briskly until dry. Recommended for repeated use. children under 6 years of age should be supervised when using this product.

Directions Spray enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Recommended for repeated use. Children under 6 years of age should be supervised when using this product.

⚠️ Warnings ~2 min read ▾

Warnings For external use only. Flammable, keep away from fire or flame. Do not use • in children less than 2 months of age • on open skin wounds.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin.

Stop use and ask a doctor if irritation and rash occurs. These may be signs of serious condition. Keep out of reach of children.

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

Warnings For external use only. Flammable, keep away from fire or flame. Do not use • in children less than 2 months of age • on open skin wounds.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. avoid contact with broken skin. Stop use and ask a doctor if irritation and rash occurs.

These may be signs of serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings For external use only. Flammable, keep away from fire or flame. Do not use in children less than 2 months of age on open skin wounds.

When using this product Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and rash occurs.

These may be signs of serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings For external use only. Flammable, keep away from heat or flame. Do not use in children less than 2 months of age on open skin wounds.

When using this product Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and rash occurs.

These may be signs of serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 28 words ▾

Active ingredient Alcohol 70% v/v Purpose Antiseptic

🧪 Inactive Ingredients 117 words ▾

Inactive ingredients Water, Fragrance, Leuconostoc/Radish Root Ferment Filtrate, Glycereth-26, Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Yellow 5.

Inactive ingredients Water, Fragrance, Leuconostoc/Radish Root Ferment Filtrate, Glycereth-26, Tris (Tetramethylhydroxypiperidinol) Citrate, Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Coumarin, Linalool, Ext. Violet 2.

Inactive ingredients Water, Fragrance, Leuconostoc/Radish Root Ferment Filtrate, Glycereth-26, Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Linalool, Limonene, Yellow 5, Yellow 6.

Inactive ingredients Water, Fragrance, Leuconostoc/Radish Root Ferment Filtrate, Glycereth-26, Tris (Tetramethylhydroxypiperidinol) Citrate, Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Peel Oil, Citrus Aurantifolia (Lime) Oil, Amyl Cinnamal, Limonene, Linalool, Red 4, Red 33, Yellow 10.

🎯 Purpose 8 words ▾

Purpose Antiseptic

📄 Do Not Use 64 words ▾

Do not use • in children less than 2 months of age • on open skin wounds.

Do not use in children less than 2 months of age on open skin wounds.

📄 When Using This Product 98 words ▾

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. avoid contact with broken skin.

When using this product Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 72 words ▾

Stop use and ask a doctor if irritation and rash occurs. These may be signs of serious condition.

📄 Keep Out of Reach of Children 76 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 26 words ▾

Package Labeling: Kit Kit

Package Labeling: 72033-104-01 Citrus Grove

Package Labeling: 72033-105-01 Frosted Mint

Package Labeling: Blue Sandalwood Blue Sandalwood

Package Labeling: Vanilla Blossom Vanilla Blossom

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for ALCOHOL — the ingredient across all brands.

Top reported reactions

Completed Suicide8,270

Toxicity To Various Agents7,834

Drug Abuse6,970

Death3,070

Overdose2,495

Vomiting2,235

Fatigue2,191

Age at onset

Neonate54

Infant28

Child28

Adolescent105

Adult4,269

Elderly893

Reporter sex

Male · 48%

Female · 52%

Unknown · 0%

Serious outcomes

Death25,103

Hospitalization14,508

Disabling3,197

Reports over time (by year) — tap or hover for the count & year

Most recent year is provisional (FAERS lags ~3 months).

Where does this data come from?

Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

FDA Adverse Event Reporting System (FAERS)

About this NDC listing & data coverage

Over-the-counter (OTC) product Kit / multi-component package No longer marketed (per FDA listing data)

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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.

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.

Who lists this product with the FDA?

Touchland LLC 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.

Related NDC lookups

🧪 All Alcohol NDCsSame ingredient 🏭 All Touchland labeler NDCsLabeler code 72033 📖 Read the Alcohol drug informationUses, warnings & side effects

Touchland Hydrating Hand Sanitizer Mist ALCOHOL Kit — NDC 72033-172-00 (Billing 72033-0172-00)

NDC database record

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

RxNorm drug class

Clinical

Patient education

Supplement & herbal interactions

Pricing

Packaging — all sizes for this product

Therapeutic equivalents

Availability & generic status

Inactive Ingredients / Excipients

Inactive ingredient FAQ

Manufacturer & labeler

More NDCs from Touchland LLC labeler code 72033

FDA label — Drug Facts FDA SPL

Reported adverse events (FAERS)

Top reported reactions

Age at onset

Reporter sex

Serious outcomes

About this NDC listing & data coverage

Kit / multi-component package

Questions about this listing