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Roll On Anti Perspirant Alcohol Free ALUMINUM CHLOROHYDRATE 10 g/100mL Solution, 45 mL — NDC 20394-0752-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Roll On Anti Perspirant Alcohol Free ALUMINUM CHLOROHYDRATE 10 g/100mL Solution, 45 mL — NDC 20394-752-02 (Billing 20394-0752-02)

by Care Line Industries · 45 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of 45 mL of Roll On Anti Perspirant Alcohol Free ALUMINUM CHLOROHYDRATE 10 g/100mL Solution from Care Line Industries, marketed since Dec 2008 and currently FDA-listed. It is this product's only package size.

NDC 20394-0752-02
🏷️ FDA NDC (as labeled) 20394-752-02 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 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

NDC database record

One package, one record: these facts belong to NDC 20394-752-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
20394 labeler · 752 product · 02 package
Package marketed since
Dec 1, 2008
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 2039475202 7
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 20394-752-02
Product NDC 20394-752
11-digit billing NDC 20394075202
UNII HPN8MZW13M
Application # M019
SPL Set ID b11308b3-40f0-414b-8eab-13b68b4f1393
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2008-12-01
Route TOPICAL
Dosage form SOLUTION
Substance ALUMINUM CHLOROHYDRATE
Why two NDCs? The FDA registers this code as 20394-752-02 — 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 → 20394-0752-02. 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?

This is an over-the-counter topical solution sold as an alcohol-free roll-on antiperspirant. The active ingredient aluminum chlorohydrate is commonly used in antiperspirant products to reduce moisture on the skin. It functions as an astringent and antiperspirant agent applied directly to areas like the underarms. This product is marketed under FDA's monograph rules for over-the-counter antiperspirants.

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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
20394-0752-02 You're viewing this Main listing 45 mL in 1 BOTTLE, WITH APPLICATOR 2008-12-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Roll On Anti Perspirant Alcohol Free 10 g/100mL 10565-0066-02 Hydrox 45 ml — — FDA listed —
Freshscent Anti-Perspirant Deodorant 10 g/100mL 51824-0022-02 New 59 ml — — FDA listed —
Roll On Anti Perspirant Alcohol Free 10 g/100mLthis 20394-0752-02 Care 45 ml — — FDA listed —
Roll On Anti Perspirant Alcohol Free 10 g/100mL 53329-0069-12 Medline 45 ml — — FDA listed —
Freshscent Anti-Perspirant Deodorant 10 g/100mL 51824-0021-01 New 45 ml — — FDA listed —
Roll On Anti-Perspirant (Alcohol Free) 10 g/100mL 63517-0803-45 Cardinal 45 ml — — FDA listed —
Roll-On Antiperspirant Deodorant - Scented 10 g/100mL 39892-0807-00 O&M 45 ml — — FDA listed —
Anti-Perspirant Deodorant Roll-On Unscented 10 g/100mL 10565-0074-01 Hydrox 45 ml — — 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

🏛️
2008
On the market since
Dec 2008
📍
2026
Currently FDA-listed
18 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.

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 MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
  • 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.
  • UNII S38J6RZN16
    Hydroxyethyl cellulose is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a thickener to adjust product texture, and a film-former to create smooth coatings on tablets.
  • 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 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.

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

The official label also statesPurified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

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

LabelerCare Line Industries
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code20394
First marketedDec 2008
Product typeHuman Otc Drug
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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 4 words ▾

Use Reduces underarm wetness.

⏱️ Dosage and Administration 9 words ▾

Directions Apply to underarms. Use daily for best results.

⚠️ Warnings 50 words ▾

Warnings FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. Do not use on broken skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

🧪 Active Ingredient 8 words ▾

Active ingredient Aluminum Chlorohydrate, 10% - Anhydrous Basis

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

🎯 Purpose 2 words ▾

Purpose Antiperspirant

📄 Do Not Use 6 words ▾

Do not use on broken skin.

📄 Ask a Doctor Before Use If 10 words ▾

Ask a doctor before use if you have kidney disease.

📄 When Using This Product 16 words ▾

If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

📄 Stop Use and Ask a Doctor If 7 words ▾

Stop use if rash or irritation occurs.

📄 Keep Out of Reach of Children 6 words ▾

KEEP OUT OF REACH OF CHILDREN.

📄 Package Label / Principal Display Panel 27 words ▾

PRINCIPAL DISPLAY PANEL CareLine Roll-On Anti-Perspirant Deodorant Alcohol-Free Scented MADE IN USA Net Wt.

1.5Fl. Oz. (45 mL) Principal Display Panel - 45 mL Bottle Label

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

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 Roll On Anti Perspirant Alcohol Free (this brand).

Top reported reactions

Diarrhoea2
Acute Coronary Syndrome1
Arteriosclerosis Coronary Artery1
Arteriovenous Fistula Aneurysm1
Blood Loss Anaemia1
Burns Third Degree1
Calcinosis1

Reporter sex

11 reports

Serious outcomes

Disabling2
Death2
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 6 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.

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 Care Line Industries. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Care Line Industries 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.
← 20362-0585-01 · Chongqing 20479-0682-01 · Hometown →
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.