Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Applause Instant Hand Sanitizer 3 g/5g Gel — NDC 67858-693-09 (Billing 67858-0693-09)
by QuestSpecialty Corporation · 12 BOTTLE, PLASTIC in 1 CARTON / 424 g in 1 BOTTLE, PLASTIC
This is a package of Applause Instant Hand Sanitizer 3 g/5g Gel from QuestSpecialty Corporation, marketed since Oct 2018 and currently FDA-listed.
NDC 67858-0693-09
🏷️ FDA NDC (as labeled)
67858-693-09
billing pads the product segment with a zero
This package
Contains424 g in 1 bottle, plastic
Pack sizes5 compare ↓
Product page 67858-0693-02
Also comes in:
4 bottles 67858-693-06
12 bottles 67858-693-04
24 bottles 67858-693-02
187358 g 67858-693-07
🗂️ 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 →
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
67858-693-09
Product NDC
67858-693
11-digit billing NDC
67858069309
RxCUI
581658
UNII
3K9958V90M
UPC
0831788009158, 0831788009141
Application #
505G(a)(3)
SPL Set ID
774657f1-5c39-2fed-e053-2991aa0a9064
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2018-10-02
Route
TOPICAL
Dosage form
GEL
Substance
ALCOHOL
Quick answers
- RxCUI (RxNorm): 581658
Why two NDCs?
The FDA registers this code as 67858-693-09 — 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 → 67858-0693-09. 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 1, 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...
Patient education
Supplement & herbal interactions
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 1, 2026
💬 Questions about Instant Hand Sanitizer?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 g | 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 3, 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 |
|---|---|---|---|---|
| 67858-0693-02 67858-693-02 Main listing | 24 BOTTLE in 1 CARTON / 107 g in 1 BOTTLE | 2018-10-02 | — | Active |
| 67858-0693-04 67858-693-04 | 12 BOTTLE, PLASTIC in 1 CARTON / 212 g in 1 BOTTLE, PLASTIC | 2018-10-02 | — | Active |
| 67858-0693-06 67858-693-06 | 4 BOTTLE, PLASTIC in 1 CARTON / 3407 g in 1 BOTTLE, PLASTIC | 2018-10-02 | — | Active |
| 67858-0693-07 67858-693-07 | 187358 g in 1 DRUM | 2018-10-02 | — | Active |
| 67858-0693-09 You're viewing this | 12 BOTTLE, PLASTIC in 1 CARTON / 424 g in 1 BOTTLE, PLASTIC | 2021-01-01 | — | Active |
Pack size FAQ
What quantity is in this package?
This package is listed by the FDA — 12 bottle, plastic in 1 carton / 424 g in 1 bottle, plastic.
What NDC number is used to bill for this package of Applause Instant Hand Sanitizer 3 g/5g 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price 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/1000mL 66608-0515-05 | Kimball | 3785 ml | — | — | Discontinued | — |
| Natural Extensions Fragrance- Free Instant Hand Sanitizer 60 mL/100mL 66975-0101-02 | Benco | 251 ml | — | — | FDA listed | — |
| Applause 3 g/5gthis 67858-0693-09 | QuestSpecialty | 12 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.
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2018
On the market since
Oct 2018
📍
2026
Currently FDA-listed
8 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.
- FDA Orange Book · refreshed Sep 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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
UNII 4Q93RCW27E
A synthetic polymer made from acrylic acid that's crosslinked for stability. It acts as a thickener and gelling agent in creams and gels, helping the medicine spread evenly and maintain its texture.
-
UNII 9O3K93S3TK
Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
-
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.
3 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWater, triethanolamine, fragrance, acrylic polymer
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.- FDA label on DailyMed · label index refreshed Oct 1, 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
LabelerQuestSpecialty Corporation
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code67858
First marketedOct 2018
Product typeHuman Otc Drug
Portfolio2 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 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
📄 Other Information
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses Handwash to help decrease bacterial on the skin. Recommended for repeated use.
⏱️ Dosage and Administration ▾
Directions for Use Place a palmful ( 5 grams) of product in one hand,. Spread on both hands and rub into the skin until dry (approximately 1 to 2 minutes). Place a smaller amolunt (2.5 grams) into one hand, spread over both hands to wrist and rub into the skin until dry (approximately 30 seconds). Will air dry in 15 seconds.
⚠️ Warnings ▾
Warnings Flammable. Keep away from fire or flame. For external use only.
🧪 Active Ingredient ▾
Active Ingredient Ethyl Alcohol 60%..........Antiseptic
🧪 Inactive Ingredients ▾
Water, triethanolamine, fragrance, acrylic polymer
🎯 Purpose ▾
purpose Antiseptic
📄 Do Not Use ▾
do not use In the eyes
📄 When Using This Product ▾
When Using Do not use in or near the eyes. If contact occurs, flush eyes with water for 15 minutes. Consult physician if irritatioin persists. If swallowed, seek medical assitance or consult a poison control cener immediately.
📄 Stop Use and Ask a Doctor If ▾
Stop Use Stop use and ask a doctor if: Irritation develops. If condtion persists for more than 72 hours consult a doctor. Keep out of reach of children.
📄 Keep Out of Reach of Children ▾
Keep out of reach of children.
📄 Other Information ▾
Store below 95 o F. Close spout to avoid evaporation.
📄 Package Label / Principal Display Panel ▾
label jpg Applause Quart Applause Gallon 8 oz bottle label 55 gallon label 5 gal pail bottle label carton label
No label section mentions that — try another word, or open the full label on DailyMed below.
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 Applause (this brand).
Top reported reactions
Reporter sex
Female · 100%
Serious outcomes
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 QuestSpecialty Corporation. 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 4 other package presentations of this same product, including 4 bottles (67858-0693-06), 12 bottles (67858-0693-04), 24 bottles (67858-0693-02). 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?
QuestSpecialty Corporation 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.
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.