Home › NDC Lookup › Ingredients › Aluminum Zirconium Tetrachlorohydrex Gly › 84012-0001-02
DONNA KARAN CASHMERE MIST DEODORANT ANTI-PERSPIRANT ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 154 mg/g Stick — NDC 84012-0001-02 package photo

DONNA KARAN CASHMERE MIST DEODORANT ANTI-PERSPIRANT ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 154 mg/g Stick

by Interparfums USA, LLC. · 3 CANISTER in 1 CARTON (84012-001-02) / 50 g in 1 CANISTER
NDC 84012-0001-02
🏷️ FDA NDC (as labeled) 84012-001-02 billing pads the product segment with a zero
This package
Contains50 g in 1 canister Pack sizes2 compare ↓
Also comes in: 50 g 84012-0001-01
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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 84012-001-02
Product NDC 84012-001
11-digit billing NDC 84012000102
UNII 8O386558JE
Application # M019
SPL Set ID 0f8c1f12-57a6-f0dd-e063-6294a90a58e8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-04-08
Route TOPICAL
Dosage form STICK
Substance ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Why two NDCs? The FDA registers this code as 84012-001-02 — 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 → 84012-0001-02. 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

LabelerInterparfums USA, LLC.
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code84012
First marketedApr 2020
Product typeHuman Otc Drug
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 an over-the-counter deodorant and anti-perspirant stick applied to the skin. The active ingredient, aluminum zirconium tetrachlorohydrex gly, functions as an anti-perspirant to help reduce underarm perspiration and as a deodorant to help control body odor. This product is marketed under FDA's established OTC monograph rule for deodorant and anti-perspirant drugs rather than as an individually approved application.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 7X6O37OK2I
    A synthetic fragrance compound used as a flavoring agent or aromatic component in medicines. It adds pleasant taste or smell to make the medication more acceptable to patients.
  • UNII P01OUT964K
    A fragrant plant-derived alcohol used as a flavoring agent and fragrance component in medicines. It provides taste and aroma to make the product more pleasant to use.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII N863NB338G
    Benzyl benzoate is a liquid organic compound used as a solvent and preservative in medicines. It helps dissolve active ingredients and can extend shelf life by preventing microbial growth in liquid formulations.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII A4VZ22K1WT
    Coumarin is a fragrant organic compound derived from plants or made synthetically. It adds pleasant flavor and aroma to medicines and is used as a flavoring agent in some formulations.
  • UNII 0THT5PCI0R
    A silicone-based liquid that helps distribute active ingredients evenly throughout topical products. It acts as a solvent and emollient, allowing medicines to spread smoothly on skin while improving texture and absorption.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII 8SQ0VA4YUR
    A fragrance compound derived from natural sources, used to add pleasant scent to the medicine. It serves as a flavoring or aromatic agent to mask unpleasant tastes or improve the product's sensory appeal.
  • UNII 5M0MWY797U
    A fragrant compound derived from clove oil or made synthetically. It's used as a flavoring agent to add taste and aroma to medicines, and sometimes as a preservative to help protect the product from spoiling.
  • UNII 9XP4LC555B
    A fragrance compound derived from natural plant sources or made synthetically. It's added to medicines as a flavoring agent to mask bitter tastes and improve how the medicine smells and tastes.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII 7JNC8VN07M
    A synthetic compound made from polyethylene glycol combined with stearic acid. It acts as an emulsifier and surfactant to help mix oil and water-based ingredients and improve how the medicine spreads or dissolves.
  • UNII R199TJT95T
    A synthetic liquid derived from propylene glycol and butyl alcohol. It functions as a solvent and humectant in medicines, helping dissolve active ingredients and maintain moisture in topical or oral formulations.
  • UNII ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • UNII 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.

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

The official label also statesCYCLOPENTASILOXANE, STEARYL ALCOHOL, HYDROGENATED CASTOR OIL, PPG-14 BUTYL ETHER, DIMETHICONE, TALC, FRAGRANCE/PARFUM, SILICA, PEG-8 DISTEARATE, ALLANTOIN, MALTODEXTRIN, CORN STARCH MODIFIED, BHT, ALPHA-ISOMETHYL IONONE, BENZYL BENZOATE, CITRONELLOL, COUMARIN, GERANIOL, HEXYL CINNAMAL, HYDROXYCITRONELLAL, ISOEUGENOL, LINALOOL

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 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.
Try another pack size: 50 g
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
Lady Speed Stick Double Defense Floral Fresh - antiperspirant/deodorant 154 mg/g 35000-0397-23 COLGATE 65 g — — FDA listed —
Lady Speed Stick Double Defense Active Fresh - antiperspirant/deodorant 154 mg/g 35000-0396-23 COLGATE 65 g — — Discontinued —
Ladies Speed Stick Teen Spirit Berry Burst 154 mg/g 35000-0658-11 Colgate-Palmolive 31 g — — FDA listed —
Donna Karan Cashmere Mist Deodorant Anti-Perspirant 154 mg/gthis 84012-0001-02 Interparfums 3 canisters — — FDA listed —
Lady Speed Stick Invisible Dry Power Wild Freesia 154 mg/g 35000-0582-14 Colgate-Palmolive 39.6 g — — FDA listed —
Lady Speed Stick Invisible Dry 154 mg/g 35000-0622-14 COLGATE 39.6 g — — FDA listed —
Lady Speed Stick Invisible Dry Power Powder Fresh 154 mg/g 35000-0581-14 Colgate-Palmolive 39.6 g — — Discontinued —
Lady Speed Stick 24x7 Powder Burst 154 mg/g 35000-0716-23 COLGATE 65 g — — 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

🏛️
2020
On the market since
Apr 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.

🔬 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 DONNA KARAN CASHMERE MIST DEODORANT ANTI-PERSPIRANT (this brand).

Top reported reactions

Rash4
Erythema2
Furuncle2
Abscess Soft Tissue1
Acne1
Alopecia1
Anaphylactic Reaction1

Reporter sex

7 reports
Male · 20%
Female · 80%
Reports over time (by year) — tap or hover for the count & year
2024 2025 2026 2 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
84012-0001-01 50 g in 1 CANISTER (84012-001-01) 2020-04-08 Active
84012-0001-02 You're viewing this 3 CANISTER in 1 CARTON (84012-001-02) / 50 g in 1 CANISTER 2020-04-08 Active

Pack size FAQ

What quantity is in NDC 84012-0001-02?
NDC 84012-0001-02 is listed by the FDA — 3 canister in 1 carton / 50 g in 1 canister.
What NDC number is used to bill for this package of DONNA KARAN CASHMERE MIST DEODORANT ANTI-PERSPIRANT ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 154 mg/g Stick?
Bill NDC 84012-0001-02 — the 11-digit billing format is 84012000102. 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 84012-001-02, 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: 84012-0001-02, written without dashes as 84012000102. 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 84012-0001-02, the first segment (84012) is the labeler code FDA assigned to Interparfums USA, LLC.; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Interparfums USA, LLC.. 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 1 other package presentation of this same product, including 50 g (84012-0001-01). 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?
Interparfums USA, 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 4 words ▾

Use reduces underarm perspiration

⏱️ Dosage and Administration 5 words ▾

Directions Apply to underams only

⚠️ Warnings 47 words ▾

Warnings For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active Ingredient Aluminum Zirconium Tetrachlorohydrex Gly 15.40%

🧪 Inactive Ingredients 35 words ▾

Inactive Ingredients CYCLOPENTASILOXANE, STEARYL ALCOHOL, HYDROGENATED CASTOR OIL, PPG-14 BUTYL ETHER, DIMETHICONE, TALC, FRAGRANCE/PARFUM, SILICA, PEG-8 DISTEARATE, ALLANTOIN, MALTODEXTRIN, CORN STARCH MODIFIED, BHT, ALPHA-ISOMETHYL IONONE, BENZYL BENZOATE, CITRONELLOL, COUMARIN, GERANIOL, HEXYL CINNAMAL, HYDROXYCITRONELLAL, ISOEUGENOL, LINALOOL

🎯 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 ↗
← 84009-0816-01 · Plant 84015-0920-60 · Crinetics →
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.