Home › NDC Lookup › Ingredients › Aluminum Chlorohydrate › 87975-0001-01
Melao Antiperspirant Deodorant(Salvia and Sea Salt) Aluminum Chlorohydrate 15 g/100g Stick, 75 g — NDC 87975-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Melao Antiperspirant Deodorant(Salvia and Sea Salt) Aluminum Chlorohydrate 15 g/100g Stick, 75 g — NDC 87975-001-01 (Billing 87975-0001-01)

by Zhongke Pharmaceutical (Foshan) Co., Ltd. · 75 g in 1 BOTTLE, PLASTIC

This is a package of 75 g of Melao Antiperspirant Deodorant(Salvia and Sea Salt) Aluminum Chlorohydrate 15 g/100g Stick from Zhongke Pharmaceutical (Foshan) Co., Ltd., marketed since Sep 2026 and currently FDA-listed. It is this product's only package size.

NDC 87975-0001-01
🏷️ FDA NDC (as labeled) 87975-001-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 17, 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

NDC database record

One package, one record: these facts belong to NDC 87975-001-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87975 labeler · 001 product · 01 package
Package marketed since
Sep 7, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8797500101 1
FDA record last changed
Sep 17, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87975-001-01
Product NDC 87975-001
11-digit billing NDC 87975000101
UNII HPN8MZW13M
Application # M019
SPL Set ID 5adf19e9-b252-fe36-e063-6294a90adef3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-07
Route TOPICAL
Dosage form STICK
Substance ALUMINUM CHLOROHYDRATE
Why two NDCs? The FDA registers this code as 87975-001-01 — 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 → 87975-0001-01. 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.

Clinical

🧪 What is this product?

Melao Antiperspirant Deodorant is a topical stick product containing aluminum chlorohydrate as its active ingredient. Aluminum chlorohydrate is commonly used in antiperspirant products to reduce underarm perspiration by forming a temporary plug in sweat ducts. This is an over-the-counter monograph drug, meaning it is marketed according to FDA category rules for antiperspirants and deodorants rather than as an individually approved application. The product also includes salvia and sea salt as additional ingredients.

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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
87975-0001-01 You're viewing this Main listing 75 g in 1 BOTTLE, PLASTIC 2026-09-07 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Antiperspirant Wipe for Women 15 g/100g 71592-0001-86 FlawlessWipes, 6 packets — — FDA listed —
Melao Antiperspirant Deodorant(Classic Cologne) 15 g/100g 87975-0003-01 Zhongke 45 g — — FDA listed —
MELAO ANTIPERSPIRANT DEODORANT(SALVIA and SEA SALT) 15 g/100gthis 87975-0001-01 Zhongke 75 g — — FDA listed —
MELAO ANTIPERSPIRANT DEODORANT(PINE and SANDALWOOD) 15 g/100g 87975-0002-01 Zhongke 75 g — — FDA listed —
MELAO ANTIPERSPIRANT DEODORANT(VELVET ROSE and EBONY) 15 g/100g 87975-0004-01 Zhongke 45 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

🏛️
2026
On the market since
Sep 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.

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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • 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 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII Q1LS2UJO3A
    Ceresin is a purified mineral wax derived from ozocerite. It functions as a binding agent, thickener, and coating material in medicines to help hold ingredients together and provide texture or protective coating.
  • 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 2865993309
    Ethylhexyl palmitate is an oily chemical made from palm oil and alcohol. It acts as an emollient and skin-conditioning agent in topical medicines, helping the product spread smoothly and keeping skin soft.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII F1A0PSN10V
    Lactococcus lactis is a naturally occurring bacterium used as a probiotic ingredient. It functions as a live culture to support gut health and may help maintain digestive balance in the formulation.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • UNII NVZ4I0H58X
    A waxy substance made from sorbitol and stearic acid. It acts as an emulsifier and stabilizer, helping keep oil and water mixed together and preventing separation in the medicine.

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

The official label also statesETHYLHEXYL PALMITATE, PARAFFIN, CYCLOPENTASILOXANE, OZOKERITE,GLYCERYL STEARATE, SORBITAN STEARATE, BEESWAX, MINERAL OIL,PARFUM, BHT, PROPYLPARABEN, LACTOCOCCUS FERMENT LYSATE,BISABOLOL

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.

Manufacturer & labeler

LabelerZhongke Pharmaceutical (Foshan) Co., Ltd.
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code87975
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from Zhongke Pharmaceutical (Foshan) Co., Ltd. labeler code 87975

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 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 📄 Ask a Doctor Before Use If 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Uses Reduces underarm perspiration. Also decreases underarm sweating due to stress.

⏱️ Dosage and Administration 11 words ▾

Directions Twist base to raise stick. Apply evenly to underarms only.

⚠️ Warnings 5 words ▾

Warnings For external use only.

🧪 Active Ingredient 5 words ▾

Active Ingredients ALUMINUM CHLOROHYDRATE 15%

🧪 Inactive Ingredients 18 words ▾

Inactive ingredients ETHYLHEXYL PALMITATE, PARAFFIN, CYCLOPENTASILOXANE, OZOKERITE,GLYCERYL STEARATE, SORBITAN STEARATE, BEESWAX, MINERAL OIL,PARFUM, BHT, PROPYLPARABEN, LACTOCOCCUS FERMENT LYSATE,BISABOLOL

🎯 Purpose 2 words ▾

Purpose Antiperspirant

📄 Do Not Use 6 words ▾

Do Not Use on broken skin.

📄 Ask a Doctor Before Use If 9 words ▾

Ask Doctor before use if you have kidney disease.

📄 Stop Use and Ask a Doctor If 7 words ▾

Stop Use if rash or irritation occurs.

📄 Keep Out of Reach of Children 19 words ▾

Keep Out Of Reach Of Children If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 49 words ▾

Other information Salvia and sea salt antiperspirant deodorant stick is an effective product that utilizes natural ingredients to effectively combat sweating and odor.It is durable, free of harmful chemicals and suitable for sensitive skin users. Carry around a portable design that keeps you fresh and confident at all times.

📄 Package Label / Principal Display Panel 4 words ▾

PRINCIPAL DISPLAY PANEL LABEL

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Zhongke Pharmaceutical (Foshan) Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Zhongke Pharmaceutical (Foshan) 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.
← 87974-0101-02 · CHI 87975-0002-01 · Zhongke →
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.