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Vindicator Instant Hand Sanitizer alcohol 600 mL/1000mL Gel, 118 mL — NDC 66608-515-27 (Billing 66608-0515-27)

by Kimball Midwest · 118 mL in 1 BOTTLE

This is a package of 118 mL of Vindicator Instant Hand Sanitizer alcohol 600 mL/1000mL Gel from Kimball Midwest, no longer marketed (first marketed Mar 2010), no longer in the FDA NDC Directory, this package's marketing ended Aug 2026.

NDC 66608-0515-27
🏷️ FDA NDC (as labeled) 66608-515-27 billing pads the product segment with a zero
This package
Contains118 mL Pack sizes2 compare ↓
Product page 66608-0515-05 Also comes in: 3785 ml 66608-515-05
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 66608-515-27 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66608 labeler · 515 product · 27 package
Package marketed since
Mar 21, 2010
Package marketing ended
Aug 1, 2026
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 6660851527 9
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Aug 2026. 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) 66608-515-27
Product NDC 66608-515
11-digit billing NDC 66608051527
RxCUI 581658
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 299b7f28-de8c-403e-92f0-f7ab5b1db849
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Aug 2026)
Marketing start 2010-03-21
Marketing end 2026-08-01
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 581658
Why two NDCs? The FDA registers this code as 66608-515-27 — 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 → 66608-0515-27. 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, 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.

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.
Try another pack size: 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
66608-0515-05 66608-515-05 Main listing 3785 mL in 1 BOTTLE 2010-03-21 Aug 1, 2026 Discontinued by firm
66608-0515-27 You're viewing this 118 mL in 1 BOTTLE 2010-03-21 Aug 1, 2026 Discontinued by firm

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 118 mL — 118 ml in 1 bottle.
How does this package differ from NDC 66608-0515-05?
Both are Vindicator Instant Hand Sanitizer alcohol 600 mL/1000mL Gel — the drug itself is identical. This page's package is the 118 mL one, while NDC 66608-0515-05 is the 3785 ml package.
What NDC number is used to bill for this package of Vindicator Instant Hand Sanitizer alcohol 600 mL/1000mL Gel?
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
Isagel 600 mL/1000mL 11701-0025-45 Coloplast 800 ml — — Discontinued —
Ecolab 60 mL/100mL 47593-0507-41 Ecolab 750 ml — — FDA listed —
Ecolab Facilipro 60 mL/100mL 47593-0508-56 Ecolab 1200 ml — — FDA listed —
Ecolab Clear 60 mL/100mL 47593-0638-41 Ecolab 750 ml — — Discontinued —
SSDC Gel Hand Sanitizer 60 mL/100mL 47593-0664-70 Ecolab 1200 ml — — FDA listed —
Covex Antibacterial Hand Sanitizer, COOL BREEZE .6 mL/mL 51209-0012-00 DALAN 236 ml — — FDA listed —
Covex Antibacterial Hand Sanitizer, FRESH ALOE .6 mL/mL 51209-0013-00 DALAN 236 ml — — FDA listed —
Amcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer 600 mL/L 51801-0437-08 Nomax, 237 l — — FDA listed —
SunDrops 75 .6 mL/mL 63621-0356-14 Sunburst 3785 ml — — FDA listed —
Aire-Master Hand Sanitizer 600 mL/L 65585-0358-01 Whisk 473 l — — FDA listed —
Sani-Sure 600 mL/L 65585-0359-01 Whisk 237 l — — FDA listed —
WhiskCare 375 600 mL/L 65585-0375-01 Whisk 8 l — — Discontinued —
WhiskCare 375 Fragrance Free 600 mL/L 65585-0378-01 Whisk 8 l — — FDA listed —
Pacific Breeze Instant Hand Sanitizer Gel 600 mL/L 65585-0380-01 Whisk 1 l — — FDA listed —
D-Germ 600 mL/L 65585-0498-01 Whisk 118 l — — FDA listed —
Algonquin HanSan 600 mL/L 65585-0522-02 Whisk 237 l — — FDA listed —
Aire-Master Waterless Hand Sanitizer 600 mL/L 65585-0525-01 Whisk 8 l — — FDA listed —
Unscented Hand Sanitizer 60 mL/100mL 65692-2074-01 Raining 44 ml — — FDA listed —
Unscented Hand Sanitizer 60 mL/100mL 65692-2075-01 Raining 30 ml — — FDA listed —
Unscented Hand Sanitizer 60 mL/100mL 65692-2076-01 Raining 59 ml — — FDA listed —
Vindicator Instant Hand Sanitizer 600 mL/1000mLthis 66608-0515-27 Kimball 118 ml — — Discontinued —
Natural Extensions Fragrance- Free Instant Hand Sanitizer 60 mL/100mL 66975-0101-02 Benco 251 ml — — FDA listed —
Applause 3 g/5g 67858-0693-02 QuestSpecialty 24 bottles — — FDA listed —
Avant Original - Fragrance Free 60 mL/100mL 68306-0106-01 B4 82.5 ml — — Discontinued —
Zogics Instant Hand Sanitizer Hydrating Gel 60 mL/100mL 72202-0026-01 Zogics, 1000 ml — — FDA listed —
palm party 60 mL/100mL 87322-1614-01 Dongyang 30 ml — — FDA listed —
Clean and Go 600 mL/1000mL 87377-0001-01 Satellite 800 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

🏛️
2010
On the market since
Mar 2010
📍
2026
Currently FDA-listed
16 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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
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.

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

LabelerKimball Midwest
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code66608
First marketedMar 2010
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Kimball Midwest labeler code 66608

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 20 words ▾

Uses Helps reduce bacteria that potentially can cause disease Helps prevent cross contamination by hand contact Recommended for repeated use

⏱️ Dosage and Administration 38 words ▾

Directions Use no water or towels Apply appropriate amount of product to palm of hand Rub until hands are completely covered Agitate lightly until dry Let air dry for 15 seconds Do not rinse or wipe with towel.

⚠️ Warnings 64 words ▾

Warnings For external use only Flammable, keep away from fire, heat, or flame Keep out of reach of children. Do not use near eyes • In case of eye contact flush with water for 15 minutes • If irritation persists stop use of product and get medical attention • In case of accidental ingestion seek medical attention or contact a poison control center immediately.

🧪 Active Ingredient 5 words ▾

Active Ingredient: Ethanol (60% v/v)

🧪 Inactive Ingredients 11 words ▾

Inactive Ingredients Water, Carbomer, Triethanolamine, PEG-75 Lanolin, Aloe Vera Gel, Fragrance.

🎯 Purpose 4 words ▾

Purpose: Anti-Microbial Hand Sanitizer

📄 Keep Out of Reach of Children 51 words ▾

Keep out of reach of children. Do not use near eyes • In case of eye contact flush with water for 15 minutes • If irritation persists stop use of product and get medical attention • In case of accidental ingestion seek medical attention or contact a poison control center immediately.

📄 Package Label / Principal Display Panel 5 words ▾

Packaging Vindicator Instant Hand Sanitizer

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 — 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 3785 ml (66608-0515-05). 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?
Kimball Midwest 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.
← 66608-0216-01 · Kimball 66613-8459-01 · Rohto →
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.