Home › NDC Lookup › Ingredients › Aluminum Sesquichlorohydrate › 74307-0125-01
Carpe Antiperspirant Ocean Storm Aluminum. Sesquichlorohydrate 20 g/100g Stick, 50 g — NDC 74307-0125-01 package photo

Carpe Antiperspirant Ocean Storm Aluminum. Sesquichlorohydrate 20 g/100g Stick, 50 g

by Clutch Inc · 50 g in 1 CONTAINER (74307-125-01)
NDC 74307-0125-01
🏷️ FDA NDC (as labeled) 74307-125-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 74307-125-01
Product NDC 74307-125
11-digit billing NDC 74307012501
UNII UCN889409V
UPC 0810160271109
Application # M019
SPL Set ID 3ec5f0fb-e493-61ec-e063-6294a90a5368
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 STICK
Substance ALUMINUM SESQUICHLOROHYDRATE
Why two NDCs? The FDA registers this code as 74307-125-01 — 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 → 74307-0125-01. 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

LabelerClutch Inc
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code74307
First marketedSep 2025
Product typeHuman Otc Drug
Portfolio23 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 an over-the-counter antiperspirant stick applied to the skin. The active ingredient, aluminum sesquichlorohydrate, is commonly used in antiperspirant products to reduce underarm perspiration. This product is marketed as an OTC monograph drug, meaning it follows FDA's established safety and effectiveness guidelines for antiperspirant ingredients rather than being individually reviewed and approved through a separate application process.

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 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.
  • UNII LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII E4F12ROE70
    A refined mineral oil derived from crude petroleum containing 13 to 14 carbon chains. It acts as a solvent, emollient, and carrier in topical formulations to help dissolve active ingredients and improve product texture and spreadability.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII YRC528SWUY
    A waxy emulsifier made from plant-derived fatty alcohols. It helps blend oil and water-based ingredients together and improves how the medicine spreads and absorbs.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII ISE9I7DNUG
    Cocoglycerides are fatty substances derived from coconut oil. They act as emulsifiers and solubilizers in medicines, helping blend water and oil-based ingredients together and improve how the body absorbs certain drugs.
  • 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • UNII NT00Y05A2V
    A liquid extract from witch hazel plant leaves and twigs. It's used in topical products as an astringent agent and to help deliver other active ingredients into the skin.
  • 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 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • 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.
  • UNII U27K0H1H2O
    Sage oil is a plant-derived liquid extracted from sage leaves. It's used in medicines as a flavoring agent and preservative to improve taste and help protect the product from spoilage.
  • 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 87WR3BHC09
    Sodium caproyl lactylate is a compound made from lactic acid and a fatty acid. It works as an emulsifier and preservative to help keep ingredients mixed together and prevent spoilage in the medicine.
  • UNII 8Z96QXD6UM
    Triethyl citrate is a clear liquid derived from citric acid. It acts as a plasticizer and solvent in tablet coatings and film formulations, helping the coating remain flexible and adhere properly to the medicine.
  • 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.

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

The official label also statesWater, C13-14 Isoalkane, Silica, Cetearyl Alcohol, Glyceryl Monostearate SE, Silica Silylate, Ethyhexyl Palmitate, Propylene Glycol, Zea Mays (Corn) Starch, Aminomethyl Propanol, Ceteareth-20, Hamamelis Virginiana (Witch Hazel) Water, Fragrance, Coco Glycerides, Salvia Officinalis (Sage) Oil, Sodium Caproyl/Lauroyl Lactylate, Triethyl Citrate, Phenoxyethanol, Alcohol, Caprylyl Glycol, Polysorbate 20

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.
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
Carpe Antiperspirant Ocean Storm 20 g/100gthis 74307-0125-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Citrus and Salt 20 g/100g 74307-0237-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Amber Glow 20 g/100g 74307-0161-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Amber Dusk 20 g/100g 74307-0169-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Mountain Breeze 20 g/100g 74307-0823-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Rose Water 20 g/100g 74307-0817-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Sandalwood 20 g/100g 74307-0821-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Bourbon Pepper 20 g/100g 74307-0159-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Fragrance Free 20 g/100g 74307-0815-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Cucumber Spa 20 g/100g 74307-0811-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Fresh Powder 20 g/100g 74307-0829-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Ocean Storm 20 g/100g 74307-0171-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Lavender Citrus 20 g/100g 74307-0819-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Coconut Vanilla 20 g/100g 74307-0825-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Clean Sport 20 g/100g 74307-0827-01 Clutch 50 g — — FDA listed —
Carpe Antiperspirant Birchwood and Lavender 20 g/100g 74307-0163-01 Clutch 50 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
74307-0125-01 You're viewing this 50 g in 1 CONTAINER (74307-125-01) 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 74307-125-01, 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: 74307-0125-01, written without dashes as 74307012501. 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 74307-0125-01, the first segment (74307) is the labeler code FDA assigned to Clutch Inc; the middle segment (0125) 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 Clutch Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Clutch Inc 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 3 words ▾

Reduces underarm perspiration.

⏱️ Dosage and Administration 25 words ▾

Apply to underarms only Rotate knob to dispense product and rub in vigorously Apply every night before going to bed and again in the morning

⚠️ Warnings 33 words ▾

For external use only. Do not use on broken or irritated skin Stop use and ask a doctor if rash or irritation occurs Ask a doctor before use if you have kidney disease

🧪 Active Ingredient 3 words ▾

Aluminum Sesquichlorohydrate 20%

🧪 Inactive Ingredients 45 words ▾

Water, C13-14 Isoalkane, Silica, Cetearyl Alcohol, Glyceryl Monostearate SE, Silica Silylate, Ethyhexyl Palmitate, Propylene Glycol, Zea Mays (Corn) Starch, Aminomethyl Propanol, Ceteareth-20, Hamamelis Virginiana (Witch Hazel) Water, Fragrance, Coco Glycerides, Salvia Officinalis (Sage) Oil, Sodium Caproyl/Lauroyl Lactylate, Triethyl Citrate, Phenoxyethanol, Alcohol, Caprylyl Glycol, Polysorbate 20

🎯 Purpose 1 words ▾

Anti-perspirant

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 74307-0012-01 · Clutch 74307-0159-01 · Clutch →
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.