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Justice Cucumber And Melon Scented Anti-bacterial Hand Sanitizer ALCOHOL 620 mg/mL Gel, 30 mL — NDC 60637-0140-30 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Justice Cucumber And Melon Scented Anti-bacterial Hand Sanitizer ALCOHOL 620 mg/mL Gel, 30 mL — NDC 60637-140-30 (Billing 60637-0140-30)

by Tween Brands, Inc. · 30 mL in 1 BOTTLE, PLASTIC

This is a package of 30 mL of Justice Cucumber And Melon Scented Anti-bacterial Hand Sanitizer ALCOHOL 620 mg/mL Gel from Tween Brands, Inc., marketed since Feb 2020 and currently FDA-listed. It is this product's only package size.

NDC 60637-0140-30
🏷️ FDA NDC (as labeled) 60637-140-30 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 60637-140-30
Product NDC 60637-140
11-digit billing NDC 60637014030
RxCUI 1020119
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 7823d0de-880e-4c56-acc7-b5c03dbf0e7a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-02-06
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1020119
Why two NDCs? The FDA registers this code as 60637-140-30 — 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 → 60637-0140-30. 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 Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants
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

📗 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 →

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.

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 gPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
60637-0140-30 You're viewing this Main listing 30 mL in 1 BOTTLE, PLASTIC 2020-02-06 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Watermelon Wonder Hand Sanitizer 620 mg/g 11673-0768-30 Target 30 g — — FDA listed —
Justice Cucumber And Melon Scented Anti-bacterial Hand Sanitizer 620 mg/mLthis 60637-0140-30 Tween 30 ml — — FDA listed —
Justice Rainbow Berry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0141-30 Tween 30 ml — — FDA listed —
Justice Rainbow Peach Mango Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0142-30 Tween 30 ml — — FDA listed —
Justice Vanilla Sprinkles Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0143-30 Tween 30 ml — — FDA listed —
Justice Watermelon and Strawberry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0144-30 Tween 30 ml — — FDA listed —
melon mango melt hand sanitizer 620 mg/mL 11673-0863-15 Target 15 ml — — FDA listed —
Justice Cranberry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0117-30 Tween 30 ml — — FDA listed —
Justice Glitter Berry Scented Anti-bacterial Hand Sanitizer A 620 mg/mL 60637-0118-30 Tween 30 ml — — FDA listed —
Justice Glitter Berry Scented Anti-bacterial Hand Sanitizer Llama 620 mg/mL 60637-0119-30 Tween 30 ml — — FDA listed —
Justice Bubbling Blueberry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0120-30 Tween 30 ml — — FDA listed —
Justice Sparkling Strawberry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0121-30 Tween 30 ml — — FDA listed —
Justice Vanilla Vibes Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0122-30 Tween 30 ml — — FDA listed —
Justice Confetti Cupcake Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0123-30 Tween 30 ml — — FDA listed —
Justice Rainbow Raspberry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0124-30 Tween 30 ml — — FDA listed —
Justice Moonstone Melon Scented Antibacterial Hand Sanitizer 620 mg/mL 60637-0191-30 Tween 30 ml — — FDA listed —
Justice Amazing Melon Scented Antibacterial Hand Sanitizer 620 mg/mL 60637-0192-30 Tween 30 ml — — FDA listed —
Justice Rainbow Raspberry Scented Antibacterial Hand Sanitizer 620 mg/mL 60637-0193-30 Tween 30 ml — — FDA listed —
Justice Diamond Vanilla Scented Antibacterial Hand Sanitizer 620 mg/mL 60637-0194-30 Tween 30 ml — — FDA listed —
Justice be Happy Citrus Scented Antibacterial Hand Sanitizer 620 mg/mL 60637-0195-30 Tween 30 ml — — FDA listed —
Justice Vanilla Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0227-30 TWEEN 30 ml — — FDA listed —
Justice Berry Scented Anti-bacterial Hand Sanitizer BFF 620 mg/mL 60637-0228-30 Tween 30 ml — — FDA listed —
Justice Cotton Candy Scented Anti-bacterial Hand Sanitizer Cat 620 mg/mL 60637-0229-30 Tween 30 ml — — FDA listed —
Justice Berry Scented Anti-bacterial Hand Sanitizer 620 mg/mL 60637-0230-00 Tween 30 ml — — FDA listed —
Justice Cotton Candy Scented Anti bacterial Hand Sanitizer 620 mg/mL 60637-0231-00 Tween 30 ml — — FDA listed —
Justice Grape Scented Anti bacterial Hand Sanitizer 620 mg/mL 60637-0232-00 Tween 30 ml — — FDA listed —
Justice Flamingo Berry Scented Anti bacterial Hand Sanitizer 620 mg/mL 60637-0300-30 Tween 30 ml — — FDA listed —
Justice Sweet Pineapple Scented Anti bacterial Hand Sanitizer 620 mg/mL 60637-0301-30 Tween 30 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70204-0100-30 Hit 30 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70412-0131-15 Zhejiang 15 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70412-0132-15 Zhejiang 15 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70412-0133-15 Zhejiang 15 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70412-0134-15 Zhejiang 15 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70412-0135-15 Zhejiang 15 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 70412-0190-15 Zhejiang 15 ml — — FDA listed —
Antiseptic Hand Rub 620 mg/mL 39892-0412-01 O&M 1.5 ml — — FDA listed —
Hand Sanitizer 620 mg/mL 71160-0110-40 Tekweld 40 ml — — FDA listed —
Antibacterial Hand Sanitizer 620 mg/mL 71160-0180-29 TEKWELD 29 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
Feb 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 LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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.

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

The official label also statesWater, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl Propanol, Mica, Yellow 5, Blue 1.

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

LabelerTween Brands, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code60637
First marketedFeb 2020
Product typeHuman Otc Drug
Portfolio20 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.

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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Use for hand-washing to decrease bacteria on the skin, Recommended for repeated area

⏱️ Dosage and Administration 20 words ▾

Directions wet hands thoroughly with product and allow to dry without wiping Supervise children in the use of this product.

⚠️ Warnings 90 words ▾

Warnings Flammable, keep away from fire or flames For external use only Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animals bites, or serious burns, consult a doctor. Use only as directed.

Do not drink. If taken internally, it will produce serious gastric disturbances. Stop use and ask a doctor if Irritation persists for more than 72 hours.

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

🧪 Active Ingredient 6 words ▾

Active ingredient Alcohol 62% Purpose Antiseptic

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl Propanol, Mica, Yellow 5, Blue 1.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Do Not Use 45 words ▾

Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animals bites, or serious burns, consult a doctor. Use only as directed. Do not drink. If taken internally, it will produce serious gastric disturbances.

📄 Stop Use and Ask a Doctor If 14 words ▾

Stop use and ask a doctor if Irritation persists for more than 72 hours.

📄 Keep Out of Reach of Children 19 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 3 words ▾

Package Labeling: Label

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

0 reports
Male · 48%
Female · 52%
Unknown · 0%

Serious outcomes

Hospitalization14,508
Life-threatening4,437
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 3,787 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.

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 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.
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 Tween Brands, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Tween Brands, 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.
← 60637-0124-30 · Tween 60637-0141-30 · Tween →
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.