NDC 73306-1175-01 — ABOVE EXTREME MEN BLACK ANTIPERSPIRANT MAXX

🆔 Identity & classification

FDA NDC (as labeled) 73306-1175-1

Product NDC 73306-1175

11-digit billing NDC 73306117501

UNII UCN889409V

Application # M019

SPL Set ID 18bc4f03-7d0c-5294-e063-6394a90aa522

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2024-05-18

Route TOPICAL

Dosage form AEROSOL, SPRAY

Substance ALUMINUM SESQUICHLOROHYDRATE

Why two NDCs? The FDA registers this code as 73306-1175-1 — 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 → 73306-1175-01. 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

LabelerBASTON INDUSTRIA DE AEROSSOIS LTDA

FDA applicationM019 (OTC MONOGRAPH DRUG)

Labeler code73306

First marketedMay 2024

Product typeHuman Otc Drug

Portfolio43 products on file

🔎 All NDCs from BASTON INDUSTRIA DE AEROSSOIS LTDA

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 antiperspirant spray marketed as a 72-hour formula under FDA's OTC monograph rules for antiperspirant products. The active ingredient, aluminum sesquichlorohydrate, is commonly used in antiperspirants to reduce underarm moisture by temporarily blocking sweat ducts. The product is applied topically as an aerosol spray to the skin.

Patient education

📘 MedlinePlus patient leaflet ↗

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.

💊 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.

UNII A8289P68Y2
Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesBUTANE (BUTANO) PROPANE (PROPANO) ISOBUTANE (ISOBUTANO) ISOPROPYL MYRISTATE ISODODECANE ALUMINUM SESQUICHOLOHYDRATE PARFUM (PERFUME) AQUA PPG-14 BUTYL ETHER (ÉTER BUTÍLICO PPG-14) QUATERNIUM-18 HECTORITE 2-METHYL 5-CYCLOHEXYLPENTANOL (2-METIL 5-CICLOEXILPENTANOL) PROPYLENE CARBONATE TOCOPHERYL ACETATE (ACETATO DE DEXTROALFATOCOFEROL) GOSSYPIUM HERBACEUM SEED OIL BUTYROSPERMUM PARKII BUTTER MACADAMIA TERNIFOLIA SEED OIL COCOS NUCIFERA FRUIT EXTRACT CHAMOMILLA RECUTITA FLOWER EXTRACT ALOE BARBADENSIS LEAF EXTRACT CAMELLIA SINENSIS LEAF EXTRACT CINNAMOMUM ZEYLANICUM BARK EXTRACT COMMIPHORA MYRRHA RESIN EXTRACT OLEA EUROPAEA FRUIT OIL ARGANIA SPINOSA KERNEL OIL LECITHIN (LECITINA) POLYGLYCERYL-3 DIISOSTEARATE GLYCERIN (GLICEROL) GLYCERYL STEARATE

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 mL	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.

🔁 Therapeutic equivalents

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Above Extreme Men Black Antiperspirant Maxx 72H 19.2 mg/150gthis 73306-1175-01	BASTON	150 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

May 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.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
73306-1175-01 You're viewing this	150 g in 1 BOTTLE, SPRAY (73306-1175-1)	2024-05-18	Active

🧭 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 73306-1175-1, 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: 73306-1175-01, written without dashes as 73306117501. 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 73306-1175-01, the first segment (73306) is the labeler code FDA assigned to BASTON INDUSTRIA DE AEROSSOIS LTDA; the middle segment (1175) 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.

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 BASTON INDUSTRIA DE AEROSSOIS LTDA. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

BASTON INDUSTRIA DE AEROSSOIS LTDA 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 and Cautions ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose

🎯 Indications and Usage 36 words ▾

Shake the container well and apply to the underarms approximately 15cm away. Protect the eyes during the application Shake the container well and apply to the underarms approximately 15cm away. Protect the eyes during the application

⏱️ Dosage and Administration 6 words ▾

UNDERARM ANTIPERSPIRANT DEODORANT UNDERARM ANTIPERSPIRANT DEODORANT

⚠️ Warnings and Cautions ~2 min read ▾

FLAMMABLE. DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH.

KEEP AWAY FROM FACE AND MOUTH TO AVOID BREATHING IN. AVOID SPRAYING IN EYES. CONTENTS UNDER PRESSURE.

DO NOT PUNCTURE OR INCINERATE. DO NOT EXPOSE TO HEAT, SUNLIGHT OR STORE AT TEMPERATURES ABOVE 120°F/50°C OR IN ENCLOSED PLACES THAT COULD OVERHEAT. DO NOT USE ON BROKEN SKIN.

STOP USE IF RASH OR IRRITATION OCCURS. GET MEDICAL ATTENTION IMMEDIATELY. ASK A DOCTOR BEFORE USING IF YOU HAVE KIDNEY DISEASE.

KEEP OUT OF REACH OF CHILDREN AND ANIMALS. USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.

AVOID THE INHALATION OF THE PRODUCT. IN CASE OF CONTACT WITH EYES, RINSE WITH PLENTY OF WATER. IF SWALLOWED, DO NOT INDUCE VOMITING; CONSULT YOUR HEALTHCARE PROVIDER IMMEDIATELY.

DO NOT LEAVE THE AEROSOL CONTAINER IN A VEHICLE. RISK OF LEAKAGE AND EXPLOSION. CONTAINER MATERIAL: STEEL.

BATCH AND EXPIRATION ON THE BOTTOM OF THE CONTAINER. HELP STOP INHALATION ABUSE: WWW.INHALANT.ORG FLAMMABLE. DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING.

CAN CAUSE SERIOUS INJURY OR DEATH. KEEP AWAY FROM FACE AND MOUTH TO AVOID BREATHING IN. AVOID SPRAYING IN EYES.

CONTENTS UNDER PRESSURE. DO NOT PUNCTURE OR INCINERATE. DO NOT EXPOSE TO HEAT, SUNLIGHT OR STORE AT TEMPERATURES ABOVE 120°F/50°C OR IN ENCLOSED PLACES THAT COULD OVERHEAT.

DO NOT USE ON BROKEN SKIN. STOP USE IF RASH OR IRRITATION OCCURS. GET MEDICAL ATTENTION IMMEDIATELY.

ASK A DOCTOR BEFORE USING IF YOU HAVE KIDNEY DISEASE. KEEP OUT OF REACH OF CHILDREN AND ANIMALS. USE ONLY AS DIRECTED.

INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL. AVOID THE INHALATION OF THE PRODUCT. IN CASE OF CONTACT WITH EYES, RINSE WITH PLENTY OF WATER.

IF SWALLOWED, DO NOT INDUCE VOMITING; CONSULT YOUR HEALTHCARE PROVIDER IMMEDIATELY. DO NOT LEAVE THE AEROSOL CONTAINER IN A VEHICLE. RISK OF LEAKAGE AND EXPLOSION.

CONTAINER MATERIAL: STEEL. BATCH AND EXPIRATION ON THE BOTTOM OF THE CONTAINER. HELP STOP INHALATION ABUSE: WWW.INHALANT.ORG

⚠️ Warnings ~2 min read ▾