Home › NDC Lookup › Ingredients › Alcohol › 65321-0036-01
TC Enriched Foam Alcohol Hand Sanitizer 70 mg/100mL Liquid — NDC 65321-0036-01 package photo

TC Enriched Foam Alcohol Hand Sanitizer 70 mg/100mL Liquid

by Rubbermaid Commercial Products LLC · 4 POUCH in 1 BOX (65321-036-01) / 1000 mL in 1 POUCH
NDC 65321-0036-01
🏷️ FDA NDC (as labeled) 65321-036-01 billing pads the product segment with a zero
This package
Contains1000 mL in 1 pouch Pack sizes4 compare ↓
Also comes in: 4 pouches 65321-0036-02 4 pouches 65321-0036-03 4 pouches 65321-0036-04
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

🆔 Identity & classification

FDA NDC (as labeled) 65321-036-01
Product NDC 65321-036
11-digit billing NDC 65321003601
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 4f3f0d3f-39c6-4ad4-9cb0-6e0d7b568e51
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2019-11-04
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 65321-036-01 — 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 → 65321-0036-01. 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.

🏭 Manufacturer & labeler

LabelerRubbermaid Commercial Products LLC
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code65321
First marketedNov 2019
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

📗 Our plain-language guide HelloPharmacist
  • Chemically they are related, but hand sanitizer is absolutely not safe to drink — it contains alcohol in concentrations that are toxic if swallowed and often includes other ingredi...
  • Is the alcohol in hand sanitizer the same as the alcohol in a drink?
  • Yes — most of these products are specifically labeled 'recommended for repeated use.' Just apply enough to cover your hands and rub until dry. If you notice skin irritation or redn...
  • Can I use hand sanitizer over and over throughout the day?
📖 Read our full Alcohol guide →

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 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII GO50W2HWO8
    A synthetic liquid made from plant oils and polyethylene glycol. It works as a solvent and emulsifier to help dissolve and mix active ingredients evenly throughout the medicine.
  • UNII 2KAG279R6R
    Dehydroacetic acid is a synthetic preservative that prevents mold, yeast, and bacterial growth in medicines. It extends shelf life by protecting the product from spoilage during storage and use.
  • UNII 0K5Y9U1P6M
    A synthetic compound combining vitamin E derivative with fatty acid chemistry, used as an antioxidant and preservative to prevent ingredient degradation and extend shelf life in medications.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII ND6MYD0T84
    A silicone-based compound mixed with polyethylene glycol and polypropylene glycol. It acts as an emulsifier and surfactant to help blend oil and water components, and reduces foaming in liquid medicines and topical products.
  • 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 2126FD486L
    Polyethylene oxide 600000 is a synthetic polymer derived from ethylene. It acts as a binder and thickener in medicines, helping hold ingredients together and control how quickly the drug dissolves or releases.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • UNII TU7HW0W0QT
    A salt derived from lactic acid, sodium lactate acts as a buffer and pH stabilizer in medicines. It helps maintain the product's acidity level and can also serve as a humectant to retain moisture.
  • 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.

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

The official label also statesWater (Aqua), PEG-6 Caprylic/Capric Glycerides, Sodium Lactate, PEG-14M, Silica, Disodium Lauriminodipropionate Tocopheryl Phosphates, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid, PEG/PPG-25/25 Dimethicone, Shea Butteramidopropyl Betaine, Hexylene Glycol, Sodium Citrate, Lactic Acid

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: 4 pouches 4 pouches 4 pouches
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
B-Pure Moisturizing Hand Sanitizer Pumpkin Vanilla Scented 70 mg/100mL 80684-0157-00 FOURSTAR 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Mocha Coffee Scented 70 mg/100mL 80684-0163-01 FOURSTAR 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Cherry Burst Scented 70 mg/100mL 80684-0162-01 FOURSTAR 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Almond Vanilla Scented 70 mg/100mL 80684-0161-01 FOURSTAR 34 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Sweet Blueberry Scented 70 mg/100mL 80684-0164-01 FOURSTAR 34 ml — — FDA listed —
B-Pure Hand Sanitizer Ginger Citrus Scented 70 mg/100mL 80684-0160-01 FOURSTAR 10 ml — — FDA listed —
B-Pure Hand Sanitizer Pumpkin Scented 70 mg/100mL 80684-0158-01 FOURSTAR 10 ml — — FDA listed —
B-Pure Moisturizing Hand Sanitizer Honey Crisp Apple Scented 70 mg/100mL 80684-0156-00 FOURSTAR 34 ml — — FDA listed —
B-Pure Hand Sanitizer Sugar Cookie Scented 70 mg/100mL 80684-0159-01 FOURSTAR 10 ml — — FDA listed —
TC Enriched Foam Alcohol Hand Sanitizer 70 mg/100mLthis 65321-0036-01 Rubbermaid 4 pouches — — 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

🏛️
2019
On the market since
Nov 2019
📍
2026
Currently FDA-listed
7 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.

🔬 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 TC Enriched Foam Alcohol Hand Sanitizer (this brand).

Top reported reactions

Toxicity To Various Agents6,004
Completed Suicide5,432
Drug Abuse5,289
Overdose1,887
Death1,594
Intentional Overdose1,541
Cardio-respiratory Arrest1,345

Age at onset

Neonate26
Infant14
Child16
Adolescent92
Adult2,810
Elderly294

Reporter sex

26,729 reports
Male · 55%
Female · 45%
Unknown · 0%

Serious outcomes

Death15,128
Life-threatening1,403
Disabling212
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,655 0
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
65321-0036-01 You're viewing this 4 POUCH in 1 BOX (65321-036-01) / 1000 mL in 1 POUCH 2019-11-04 Active
65321-0036-02 4 POUCH in 1 BOX (65321-036-02) / 1000 mL in 1 POUCH 2019-11-04 Active
65321-0036-03 4 POUCH in 1 BOX, UNIT-DOSE (65321-036-03) / 1000 mL in 1 POUCH 2022-03-03 Active
65321-0036-04 4 POUCH in 1 BOX (65321-036-04) / 500 mL in 1 POUCH 2022-09-12 Active

Pack size FAQ

What quantity is in NDC 65321-0036-01?
NDC 65321-0036-01 is listed by the FDA — 4 pouch in 1 box / 1000 ml in 1 pouch.
What NDC number is used to bill for this package of TC Enriched Foam Alcohol Hand Sanitizer 70 mg/100mL Liquid?
Bill NDC 65321-0036-01 — the 11-digit billing format is 65321003601. 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 65321-036-01, 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: 65321-0036-01, written without dashes as 65321003601. 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 65321-0036-01, the first segment (65321) is the labeler code FDA assigned to Rubbermaid Commercial Products LLC; the middle segment (0036) 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 Rubbermaid Commercial Products LLC. 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 4 pouches (65321-0036-02), 4 pouches (65321-0036-03), 4 pouches (65321-0036-04). 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?
Rubbermaid Commercial Products 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.

📄 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 8 words ▾

Use To decrease potentially harmful germs on skin.

⏱️ Dosage and Administration 16 words ▾

Directions Apply generously to hands. Rub hands together. Allow hands to dry. Repeat daily as necessary.

⚠️ Warnings 63 words ▾

Warnings Flammable. Keep away from fire or flame. For external use only. When using this product avoid contact with eyes. In case of eye contact, flush 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. If swallowed, do not induce vomiting, get medical attention.

🧪 Active Ingredient 6 words ▾

Active ingredient Alcohol Denat. 75% (v/v)

🧪 Inactive Ingredients 31 words ▾

Inactive ingredients Water (Aqua), PEG-6 Caprylic/Capric Glycerides, Sodium Lactate, PEG-14M, Silica, Disodium Lauriminodipropionate Tocopheryl Phosphates, Phenoxyethanol, Benzoic Acid, Dehydroacetic Acid, PEG/PPG-25/25 Dimethicone, Shea Butteramidopropyl Betaine, Hexylene Glycol, Sodium Citrate, Lactic Acid

🎯 Purpose 3 words ▾

Purpose Antiseptic cleanser

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 65321-0032-01 · Rubbermaid 65321-0039-01 · Rubbermaid →
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.