palm party Alcohol Gel 60 mL/100mL Gel, 100 mL
by Dongyang Loulee Cosmetics Co.,Ltd. · 100 mL in 1 CARTON (87322-1614-4)
NDC 87322-1614-04
🏷️ FDA NDC (as labeled)
87322-1614-4
billing pads the package segment with a zero
This package
Contains100 mL
Pack sizes4 compare ↓
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 →
🆔 Identity & classification
FDA NDC (as labeled)
87322-1614-4
Product NDC
87322-1614
11-digit billing NDC
87322161404
RxCUI
581658
UNII
3K9958V90M
Application #
M003
SPL Set ID
487c4724-b618-a071-e063-6394a90aa782
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-01-16
Route
TOPICAL
Dosage form
GEL
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 87322-1614-4 — a 5-4-1 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 package segment → 87322-1614-04. 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.
🏭 Manufacturer & labeler
LabelerDongyang Loulee Cosmetics Co.,Ltd.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code87322
First marketedJan 2026
Product typeHuman Otc Drug
Portfolio3 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?
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.
💬 Questions about Alcohol Gel?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.
🧪 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.
-
0.2 mL / 100 mL
UNII 8Z5ZAL5H3V
A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
-
0.2 mL / 100 mL
UNII 94ZLA3W45F
Arginine is an amino acid used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level and stability of liquid formulations.
-
5 mL / 100 mL
UNII 5EM498GW35
A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
-
0.4 mL / 100 mL
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.
-
34.2 mL / 100 mL
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.
5 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWATER, FRAGRANCE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ARGININE, PHENOXYETHANOL
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 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
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
| 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/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/100mLthis 87322-1614-04 | Dongyang | 100 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
🏛️
2026
On the market since
Jan 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.
🔬 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 palm party (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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 87322-1614-01 | 30 mL in 1 CARTON (87322-1614-1) | 2026-01-16 | Active |
| 87322-1614-02 | 35 mL in 1 CARTON (87322-1614-2) | 2026-01-16 | Active |
| 87322-1614-03 | 42 mL in 1 CARTON (87322-1614-3) | 2026-01-16 | Active |
| 87322-1614-04 You're viewing this | 100 mL in 1 CARTON (87322-1614-4) | 2026-01-16 | Active |
You're viewing the largest of 4 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 87322-1614-04?
NDC 87322-1614-04 contains 100 mL — 100 ml in 1 carton.
What is the difference between NDC 87322-1614-04 and NDC 87322-1614-01?
Both are palm party Alcohol Gel 60 mL/100mL Gel — the drug itself is identical. NDC 87322-1614-04 is the 100 mL package, while NDC 87322-1614-01 is the 30 ml package.
What NDC number is used to bill for this package of palm party Alcohol Gel 60 mL/100mL Gel?
Bill NDC 87322-1614-04 — the 11-digit billing format is 87322161404. 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 87322-1614-4, 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: 87322-1614-04, written without dashes as 87322161404. 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 87322-1614-04, the first segment (87322) is the labeler code FDA assigned to Dongyang Loulee Cosmetics Co.,Ltd.; the middle segment (1614) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) 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 Dongyang Loulee Cosmetics Co.,Ltd.. 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 30 ml (87322-1614-01), 35 ml (87322-1614-02), 42 ml (87322-1614-03). 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?
Dongyang Loulee Cosmetics Co.,Ltd. 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 ▾
Uses Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
⏱️ Dosage and Administration ▾
Directions Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
⚠️ Warnings ▾
Warnings Flammable. Keep away from fire or flame. For external use only.
🧪 Active Ingredient ▾
Active ingredient(s) Alcohol 60%
🧪 Inactive Ingredients ▾
Inactive ingredients WATER, FRAGRANCE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ARGININE, PHENOXYETHANOL
🎯 Purpose ▾
Purpose(s) Antisepti
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 ↗
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.