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87066-5912 Aluminum Chlorohydrate Spray 15 g/100g Spray, 1 g — NDC 87066-5912-01 package photo

87066-5912 Aluminum Chlorohydrate Spray 15 g/100g Spray, 1 g

by Hubei Redrui Building Materials Co., Ltd. · 1 g in 1 CARTON (87066-5912-1)
NDC 87066-5912-01
🏷️ FDA NDC (as labeled) 87066-5912-1 billing pads the package segment with a zero
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) 87066-5912-1
Product NDC 87066-5912
11-digit billing NDC 87066591201
UNII HPN8MZW13M
Application # M019
SPL Set ID 3e960c2b-c365-d837-e063-6394a90a7876
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-09-12
Route TOPICAL
Dosage form SPRAY
Substance ALUMINUM CHLOROHYDRATE
Why two NDCs? The FDA registers this code as 87066-5912-1 — 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 → 87066-5912-01. 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

LabelerHubei Redrui Building Materials Co., Ltd.
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code87066
First marketedSep 2025
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

🧪 What is this product?

This is a topical spray containing aluminum chlorohydrate, an active ingredient commonly used in over-the-counter antiperspirant products. Aluminum chlorohydrate typically functions as an astringent that works to reduce moisture on the skin. This product is marketed as an OTC monograph drug, meaning it follows FDA's established safety and use guidelines for antiperspirant ingredients rather than being individually reviewed as a new drug 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.

💊 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.

  • 0.5 g / 100 g UNII RUN0H01QEU
    A clear, colorless liquid that acts as a humectant and solvent in medicines. It helps keep products moist, dissolves active ingredients, and can improve texture and stability in liquid formulations.
  • 10 g / 100 g UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 0.1 g / 100 g UNII RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • 65.9719 g / 100 g 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.
  • 0.03 g / 100 g UNII L64N7M9BWR
    A positively charged salt derived from a long-chain fatty compound. It acts as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in liquid medicines and personal care products.
  • 0.0555 g / 100 g UNII 00IF91KFKQ
    A natural extract from saffron crocus flowers. Used in medicines as a coloring agent to give products a golden-yellow hue and sometimes to add subtle flavor or aroma to the formulation.
  • 0.01 g / 100 g UNII 9WLP0FA6U4
    A plant extract from Cynanchum vincetoxicum leaves, traditionally used in herbal preparations. In medicines, it may function as a natural flavoring agent, preservative, or active botanical component, depending on the formulation.
  • 0.05 g / 100 g UNII 22ADO53M6F
    A mineral salt derived from phosphoric acid, used as a buffer to maintain the pH balance of the medication and help stabilize the active ingredients.
  • 0.1 g / 100 g UNII R66Z4YW3X0
    A plant-derived or synthetic aromatic ingredient that adds pleasant smell to the medicine. Fragrances mask unpleasant tastes or odors in oral medications to make them easier to take.
  • 2 g / 100 g UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • 0.5 g / 100 g UNII 8FP93ED6H2
    Witch hazel is a plant extract made from the leaves and twigs of the witch hazel shrub. In medicines, it works as a soothing and astringent ingredient that helps reduce inflammation and tighten skin.
  • 0.255 g / 100 g UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • 0.6 g / 100 g UNII T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • 0.55 g / 100 g UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • 0.3 g / 100 g 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.
  • 0.1 g / 100 g UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • 0.2 g / 100 g UNII 5543O0CEID
    A plant-derived material from aspen bark used as a natural filler and binder in medications. It helps hold tablet ingredients together and adds bulk to the formulation.
  • 0.5125 g / 100 g UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • 3.155 g / 100 g UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 0.0001 g / 100 g UNII 57N7B0K90A
    A mineral form of silver used in some medicines as an antimicrobial agent to help prevent bacterial growth in the product during storage.
  • 0.01 g / 100 g UNII SE337SVY37
    A mineral salt used as a buffer to help maintain the medicine's pH level and prevent breakdown of active ingredients. It also acts as a thickening agent in liquid formulations.

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

The official label also statesAQUA, ALCOHOL, PROPYLENE GLYCOL, GLYCERIN, PEG-40 HYDROGENATED CASTOR OIL, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER, HYDROXYETHYLCELLULOSE, FRAGRANCE FLORAL, POPULUS TREMULOIDES BARK, CETRIMONIUM BROMIDE, ALOE BARBADENSIS LEAF JUICE, PROPANEDIOL, 1,2-BUTANEDIOL, PHENOXYETHANOL, HYDROXYACETOPHENONE, CROCUS SATIVUS FLOWER, POLYSORBATE 60, DISODIUM PHOSPHATE, CYNANCHUM VINCETOXICUM LEAF, SODIUM PHOSPHATE, SILVER CATION

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 mLPer 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
87066-5912 15 g/100gthis 87066-5912-01 Hubei 1 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

🏛️
2025
On the market since
Sep 2025
📍
2026
Currently FDA-listed
1 year 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 Chlorohydrate Spray — the ingredient across all brands.

Top reported reactions

Anaemia1
Bradycardia1
Brain Natriuretic Peptide Increased1
Cardiomyopathy1
Chest Discomfort1
Drug Toxicity1
Dyspnoea1

Reporter sex

2 reports
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
87066-5912-01 You're viewing this 1 g in 1 CARTON (87066-5912-1) 2025-09-12 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 87066-5912-1, 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: 87066-5912-01, written without dashes as 87066591201. 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 87066-5912-01, the first segment (87066) is the labeler code FDA assigned to Hubei Redrui Building Materials Co., Ltd.; the middle segment (5912) 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 Hubei Redrui Building Materials Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Hubei Redrui Building Materials 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 4 words ▾

Uses Reduces underarm wetness

⏱️ Dosage and Administration 23 words ▾

Directions Apply to underarms only. clean and dry skin before use. spray an appropriate amount and rub until absorbed. use 1-2 times daily

⚠️ Warnings 45 words ▾

Warnings For external use only Do not use On broken skin. if you are allergic to alcohol Ask a doctor before use if you have Kidney disease When using this product Do not get into eyes. If product gets into eyes, rinse thoroughly with water.

🧪 Active Ingredient 5 words ▾

Active ingredient Aluminum Chlorohydrate 15%

🧪 Inactive Ingredients 47 words ▾

Inactive ingredients AQUA, ALCOHOL, PROPYLENE GLYCOL, GLYCERIN, PEG-40 HYDROGENATED CASTOR OIL, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER, HYDROXYETHYLCELLULOSE, FRAGRANCE FLORAL, POPULUS TREMULOIDES BARK, CETRIMONIUM BROMIDE, ALOE BARBADENSIS LEAF JUICE, PROPANEDIOL, 1,2-BUTANEDIOL, PHENOXYETHANOL, HYDROXYACETOPHENONE, CROCUS SATIVUS FLOWER, POLYSORBATE 60, DISODIUM PHOSPHATE, CYNANCHUM VINCETOXICUM LEAF, SODIUM PHOSPHATE, SILVER CATION

🎯 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 ↗
← 87066-5827-01 · Hubei 87066-5915-01 · Hubei →
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.