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Gem Santal Aluminum Chlorohydrate 20 g/100g Aerosol, Spray, 108 g — NDC 87190-0052-00 package photo

Gem Santal Aluminum Chlorohydrate 20 g/100g Aerosol, Spray, 108 g

by Gem Products US LLC · 108 g in 1 BOTTLE, SPRAY (87190-0052-0)
NDC 87190-0052-00
🏷️ FDA NDC (as labeled) 87190-0052-0 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) 87190-0052-0
Product NDC 87190-0052
11-digit billing NDC 87190005200
UNII HPN8MZW13M
UPC 9356892001917
Application # M019
SPL Set ID 4a9663ff-dd52-0b62-e063-6394a90a3b29
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-10
Route TOPICAL
Dosage form AEROSOL, SPRAY
Substance ALUMINUM CHLOROHYDRATE
Why two NDCs? The FDA registers this code as 87190-0052-0 — 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 → 87190-0052-00. 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

LabelerGem Products US LLC
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code87190
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio9 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?

Gem Santal is an over-the-counter antiperspirant spray containing aluminum chlorohydrate, which is commonly used in topical products applied to the skin to reduce perspiration. This aerosol spray formulation delivers the active ingredient to the underarm or body surface. Aluminum chlorohydrate functions as an astringent that temporarily blocks sweat glands. This product is marketed under FDA's monograph rules for OTC antiperspirant drugs.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 6LV4FOR43R
    Butane is a colorless gas derived from petroleum. In medicines, it serves as a propellant in inhalers and aerosol sprays, helping deliver the active drug to the lungs or skin.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • 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 X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII 0B1U8K2ME0
    A synthetic gas used as a propellant in pressurized aerosol inhalers. It helps deliver the active medication as a fine mist or spray into the lungs or airways.
  • 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.
  • UNII 8D08K3S51E
    Propylene carbonate is a clear liquid solvent derived from propylene. It helps dissolve or suspend active ingredients in liquid medicines and can improve how well the product flows and mixes.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • 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.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.

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

The official label also statesBUTANE, HYDROFLUOROCARBON 152A, CYCLOPENTASILOXANE, C12-15 ALKYL BENZOATE, ZEA MAYS (CORN) STARCH, WATER (AQUA), FRAGRANCE (PARFUM), DISTEARDIMONIUM HECTORITE, TOCOPHERYLACETATE (VITAM IN E), PROPYLENE CARBONATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, CITRIC ACID, PHENOXYETHANOL, SODIUM HYALURONATE (HYALURONICACID).

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
Lume Clean Tangerine 20 g/100g 84520-0027-03 Lume 122 g — — FDA listed —
Mando Clover Woods 20 g/100g 84520-0022-04 Lume 37 g — — FDA listed —
Mando Bourbon Leather 20 g/100g 84520-0025-03 Lume 122 g — — FDA listed —
Mando Clover Woods 20 g/100g 84520-0018-03 Lume 122 g — — FDA listed —
Mando Pro Sport 20 g/100g 84520-0021-04 Lume 37 g — — FDA listed —
Lume Soft Powder 20 g/100g 84520-0013-03 Lume 122 g — — FDA listed —
Lume Lavender Sage 20 g/100g 84520-0015-03 Lume 122 g — — FDA listed —
GEM Cool Fresh 20 g/100g 87190-0051-00 Gem 108 g — — FDA listed —
Lume Clean Tangerine 20 g/100g 84520-0023-04 Lume 37 g — — FDA listed —
Lume Mint Cucumber 20 g/100g 84520-0026-03 Lume 122 g — — FDA listed —
Mando Mt Fuji 20 g/100g 84520-0028-03 Lume 122 g — — FDA listed —
Gem Coconut Vanilla 20 g/100g 87190-0049-00 Gem 108 g — — FDA listed —
Gem Vanilla Macadamia 20 g/100g 87190-0050-00 Gem 108 g — — FDA listed —
Lume Vanilla Bliss 20 g/100g 84520-0016-03 Lume 122 g — — FDA listed —
Mando Pro Sport 20 g/100g 84520-0017-03 Lume 122 g — — FDA listed —
Mando Cedar Grove 20 g/100g 84520-0019-03 Lume 122 g — — FDA listed —
Lume Soft Powder 20 g/100g 84520-0020-04 Lume 37 g — — FDA listed —
Gem Santal 20 g/100gthis 87190-0052-00 Gem 108 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
Feb 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.

🔬 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 — the ingredient across all brands.

Top reported reactions

Expired Product Administered5
Macule5
Product Administered At Inappropriate Site5
Application Site Pain4
Cervix Carcinoma4
Cervix Haemorrhage Uterine4
Erythema4

Reporter sex

40 reports
Male · 32%
Female · 66%
Unknown · 3%

Serious outcomes

Hospitalization10
Disabling6
Death3
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 17 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
87190-0052-00 You're viewing this 108 g in 1 BOTTLE, SPRAY (87190-0052-0) 2026-02-10 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 87190-0052-0, 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: 87190-0052-00, written without dashes as 87190005200. 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 87190-0052-00, the first segment (87190) is the labeler code FDA assigned to Gem Products US LLC; the middle segment (0052) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 Gem Products US LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Gem Products US 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 🆘 Overdosage 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 4 words ▾

USES REDUCES UNDERARM WTNESS

⏱️ Dosage and Administration 40 words ▾

DIRECTIONS APPLY TO UNDERARMS ONLY. SHAKE WELL. POSITION AROUND 15CM AWAY AND FROM CLEAN, DRY UNDERARMS AND SPRAY. USE EVERYDAY. DO NOT APPLY TO DAMAGED OR SORE SKIN. STOP USE IF IRRITATION DEVELOPS. DO NOT SPRAY NEAR EYES OR FACE.

⚠️ Warnings 126 words ▾

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

WHEN USING THIS PRODUCT KEEP AWAY FROM FACE AND MOUTH TO AVOID BREATHING IT. AVOID SPRAYING IN EYES. CONTENTS UNDER PRESSURE.

DO NOT PUNCTURE OR INCINERATE. DO NOT STORE AT TEMPERATURE ABOVE 120°F/50°C OR IN ENCLOSED PLACES THAT COULD OVERHEAT. USE ONLY IN A WELL-VENTILATED AREA.

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 POISON CONTROL CENTER RIGHT AWAY.

USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATLY CONCERNTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL. FOR EXTERNAL USE ONLY

🆘 Overdosage 34 words ▾

IF SWALLOWED GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY. USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATLY CONCERNTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL. FOR EXTERNAL USE ONLY

🧪 Active Ingredient 7 words ▾

ACTIVE INGREDIENTS PURPOSE Aluminum Chlorohydrate (20%) ANTIPERSPIRANT

🧪 Inactive Ingredients 35 words ▾

INACTIVE INGREDIENTS BUTANE, HYDROFLUOROCARBON 152A, CYCLOPENTASILOXANE, C12-15 ALKYL BENZOATE, ZEA MAYS (CORN) STARCH, WATER (AQUA), FRAGRANCE (PARFUM), DISTEARDIMONIUM HECTORITE, TOCOPHERYLACETATE (VITAM IN E), PROPYLENE CARBONATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, CITRIC ACID, PHENOXYETHANOL, SODIUM HYALURONATE (HYALURONICACID).

🎯 Purpose 1 words ▾

Antiperspirant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87190-0051-00 · Gem 87190-0054-00 · Gem →
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.