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Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Lavender Sage Aluminum Sesquichlorohydrate 13.2 g/75g Stick, 75 g — NDC 84520-0003-01 package photo

Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Lavender Sage Aluminum Sesquichlorohydrate 13.2 g/75g Stick, 75 g

by Lume Deodorant, LLC. · 75 g in 1 CONTAINER (84520-003-01)
NDC 84520-0003-01
🏷️ FDA NDC (as labeled) 84520-003-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ Data synced Jul 2, 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

⚠️
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 Jun 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

FDA NDC (as labeled) 84520-003-01
Product NDC 84520-003
11-digit billing NDC 84520000301
UNII UCN889409V
UPC 0850068958375, 0850074689423, 0850042058725
Application # M019
SPL Set ID 1cebcddc-fa0f-8b73-e063-6394a90ab95e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jun 2026)
Marketing start 2024-07-12
Marketing end 2026-06-30
Route TOPICAL
Dosage form STICK
Substance ALUMINUM SESQUICHLOROHYDRATE
Why two NDCs? The FDA registers this code as 84520-003-01 — 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 → 84520-0003-01. 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

LabelerLume Deodorant, LLC.
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code84520
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio27 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

🧪 What is this product?

This is a solid stick deodorant applied to the skin and marketed under FDA's over-the-counter monograph rules for antiperspirant products. The active ingredient, aluminum sesquichlorohydrate, is a common antiperspirant salt typically used to reduce underarm perspiration. The product is scented with lavender and sage fragrance and is intended for application to the body to help control moisture and odor.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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.

💲 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 eachPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Lavender Sage 13.2 g/75gthis 84520-0003-01 Lume 75 g — — Discontinued —
Lume Deodorant with Clinical Strength Sweat Control, Vanilla Bliss 13.2 g/75g 84520-0024-01 Lume 75 g — — FDA listed —
Mando - Pro Sport 13.2 g/75g 84520-0007-01 Lume 75 g — — FDA listed —
Lume Deodorant with Clinical Strength Sweat Control, Fresh Spring 13.2 g/75g 84520-0014-01 Lume 75 g — — FDA listed —
Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Unscented 13.2 g/75g 84520-0001-01 Lume 75 g — — Discontinued —
Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Soft Powder 13.2 g/75g 84520-0004-01 Lume 75 g — — FDA listed —
Mando Deodorant plus Extra Strength Sweat Control - Cedar Grove 13.2 g/75g 84520-0008-01 Lume 75 g — — FDA listed —
Lume Whole Body Deodorant Plus Sweat Control Smooth Solid, Clean Tangerine 13.2 g/75g 84520-0002-01 Lume 75 g — — Discontinued —
Mando - Mt. Fuji 13.2 g/75g 84520-0005-01 Lume 75 g — — FDA listed —
Mando - Bourbon Leather 13.2 g/75g 84520-0006-01 Lume 75 g — — Discontinued —
Mando Deodorant plus Extra Strength Sweat Control - Clover Woods 13.2 g/75g 84520-0009-01 Lume 75 g — — 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

🏛️
2024
On the market since
Jul 2024
📍
2026
Currently FDA-listed
2 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 Aluminum Sesquichlorohydrate — the ingredient across all brands.

Top reported reactions

Application Site Erythema2
Administration Site Pain1
Application Site Irritation1
Application Site Pain1
Application Site Pruritus1
Burning Sensation1
Chemical Burn1

Reporter sex

8 reports
Male · 43%
Female · 43%
Unknown · 14%
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 1 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
84520-0003-01 You're viewing this 75 g in 1 CONTAINER (84520-003-01) 2024-07-12 Discontinued by firm

🧭 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 ✓ Available
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 FDA registers it as 84520-003-01, 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: 84520-0003-01, written without dashes as 84520000301. 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 84520-0003-01, the first segment (84520) is the labeler code FDA assigned to Lume Deodorant, LLC.; the middle segment (0003) 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.
Who lists this product with the FDA?
Lume Deodorant, 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 6 words ▾

USE reduces underarm wetness extra effective

⏱️ Dosage and Administration 12 words ▾

DIRECTIONS apply to underarms only apply to dry skin apply at bedtime

⚠️ Warnings 73 words ▾

WARNINGS For external use only Do not use on broken or irritated skin Ask a doctor before use if you have kidney disease Stop use if rash or irritation occurs Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin’s sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product for a week afterwards.

🧪 Active Ingredient 5 words ▾

ACTIVE INGREDIENT Aluminum Sesquichlorohydrate 17.6%

🧪 Inactive Ingredients 35 words ▾

INACTIVE INGREDIENTS PPG-15 Stearyl Ether, Ozokerite, Neopentyl Glycol Diheptanoate, Stearyl Alcohol, Isododecane, Isopentyldiol, Lauryl Laurate, Mandelic Acid, Sorbitan Oleate, Fragrance (Parfum), Maranta Arundinacea Root Powder, Silica, Citronellyl Methylcrotonate, Zea Mays (Corn) Starch, Panthenol, Caffeine, Ethylhexylglycerin.

🎯 Purpose 2 words ▾

PURPOSE Antiperspirant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84520-0002-01 · Lume 84520-0004-01 · Lume →
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.