Home › NDC Lookup › Ingredients › Aluminum Chlorohydrate › 69423-0676-11
💨image loading
(from DailyMed)

Secret Weightless Dry White Peach plus Argan Oil Aluminum chlorohydrate 24.5 g/100g Aerosol, Spray, 116 g — NDC 69423-676-11 (Billing 69423-0676-11)

by The Procter & Gamble Manufacturing Company · 116 g in 1 CAN

This is a package of 116 g of Secret Weightless Dry White Peach plus Argan Oil Aluminum chlorohydrate 24.5 g/100g Aerosol, Spray from The Procter & Gamble Manufacturing Company, no longer marketed (first marketed Jan 2022), no longer in the FDA NDC Directory, this package's marketing ended Aug 2026. It is this product's only package size.

NDC 69423-0676-11
🏷️ FDA NDC (as labeled) 69423-676-11 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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 69423-676-11 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69423 labeler · 676 product · 11 package
Package marketed since
Jan 1, 2022
Package marketing ended
Aug 1, 2026
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 6942367611 8
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Aug 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69423-676-11
Product NDC 69423-676
11-digit billing NDC 69423067611
UNII HPN8MZW13M
Application # M019
SPL Set ID f5dd6ecc-4406-6c47-e053-2a95a90a92d3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Aug 2026)
Marketing start 2022-01-01
Marketing end 2026-08-01
Route TOPICAL
Dosage form AEROSOL, SPRAY
Substance ALUMINUM CHLOROHYDRATE
Why two NDCs? The FDA registers this code as 69423-676-11 — 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 → 69423-0676-11. 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 antiperspirant spray marketed under FDA's OTC monograph rules. The active ingredient, aluminum chlorohydrate at 24.5 percent, is commonly used in antiperspirant products to reduce underarm moisture and perspiration. The product is applied topically as an aerosol spray and is scented with peach fragrance and argan oil. It is a standard formulation in the antiperspirant category.

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
69423-0676-11 You're viewing this Main listing 116 g in 1 CAN 2022-01-01 Aug 1, 2026 Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Old Spice Fiji Dry 24.5 g/100g 84126-0035-12 The 122 g — — FDA listed —
Old Spice Swagger Scent of Cedarwood Dry 24.5 g/100g 69423-0739-01 The 2 cans — — FDA listed —
Secret Weightless Dry White Peach 24.5 g/100g 84126-0199-11 The 116 g — — FDA listed —
Secret Weightless Dry White Peach plus Argan Oil 24.5 g/100gthis 69423-0676-11 The 116 g — — Discontinued —
Secret Mango Tango Notes of Mango and Hibiscus 24.5 g/100g 84126-0261-11 The 116 g — — FDA listed —
Secret Weightless Dry Vanilla plus Argan Oil 24.5 g/100g 69423-0677-01 The 2 cans — — Discontinued —
Secret Weightless Dry Cocoa Butter 24.5 g/100g 84126-0192-11 The 116 g — — FDA listed —
Secret Berry Passionate Passionfruit and Guava 24.5 g/100g 84126-0260-11 The 116 g — — FDA listed —
Old Spice Pure Sport High Endurance Dry 24.5 g/100g 84126-0039-12 The 122 g — — FDA listed —
Secret Weightless Dry Cozy Vanilla 24.5 g/100g 84126-0195-11 The 116 g — — FDA listed —
Secret Couldnt Be Lovelier Weightless Dry Wicked for Good 24.5 g/100g 84126-0217-11 The 116 g — — FDA listed —
Dry Sweat Shield 3.5oz 24.5 g/100g 57337-0154-01 Rejoice 99 g — — FDA listed —
Old Spice Volcano with Cedar Notes Dry 24.5 g/100g 84126-0038-12 The 122 g — — FDA listed —
Dry Sweat Shield 3.5oz 24.5 g/100g 57337-0157-01 Rejoice 99 g — — FDA listed —
Secret Weightless Dry Refreshing Berry plus Argan Oil 24.5 g/100g 69423-0680-11 The 116 g — — FDA listed —
Secret Weightless Dry Waterlily plus Argan Oil 24.5 g/100g 69423-0675-11 The 116 g — — FDA listed —
Secret Weightless Dry Wild Rose plus Argan Oil 24.5 g/100g 69423-0678-01 The 2 cans — — Discontinued —
Secret Weightless Dry Cool Waterlily 24.5 g/100g 84126-0193-11 The 116 g — — FDA listed —
Secret Weightless Dry Tropical Hibiscus 24.5 g/100g 84126-0198-11 The 116 g — — FDA listed —
Secret Weightless Dry Delicate Rose 24.5 g/100g 84126-0197-11 The 116 g — — FDA listed —
Secret Weightless Dry Tropical Hibiscus plus Argan Oil 24.5 g/100g 69423-0681-11 The 116 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

🏛️
2022
On the market since
Jan 2022
📍
2026
Currently FDA-listed
4 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerThe Procter & Gamble Manufacturing Company
FDA applicationM019 (OTC MONOGRAPH DRUG)
Labeler code69423
First marketedJan 2022
Product typeHuman Otc Drug
Portfolio850 products on file

More NDCs from The Procter & Gamble Manufacturing Company labeler code 69423

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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 4 words ▾

Use reduces underarm wetness

⏱️ Dosage and Administration 5 words ▾

Directions apply to underarms only

⚠️ Warnings 83 words ▾

Warnings For external use only. Do not use on broken skin Ask a doctor before use if you have kidney disease Stop use if rash or irritation occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

When using this product keep away from face and mouth to avoid breathing it avoid spraying in eyes use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

🧪 Active Ingredient 6 words ▾

Active ingredient Aluminum chlorohydrate 24.5% (anhydrous)

🧪 Inactive Ingredients 28 words ▾

Inactive ingredients Butane, hydrofluorocarbon 152A, dimethicone, C12-15 alkyl benzoate, isopropyl myristate, PPG-14 butyl ether, fragrance, disteardimonium hectorite,mineral oil, propylene carbonate, corn starch/maltodextrin crosspolymer, dimethiconol, argania spinosa kernel oil

🎯 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 36 words ▾

When using this product keep away from face and mouth to avoid breathing it avoid spraying in eyes use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

📄 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.

📄 Questions or Comments 2 words ▾

Questions? 1-800-964-1947

📄 Package Label / Principal Display Panel 35 words ▾

PRINCIPAL DISPLAY PANEL - 116 g Can Secret ® Weightless DRY SPRAY WHITE PEACH + ARGAN OIL 48 HR SWEAT & ODOR PROTECTION ALUMINUM CHLOROHYDRATE ANTIPERSPIRANT / DEODORANT NET WT.

4.1 OZ (116 g) SEC

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 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.

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
The Procter & Gamble Manufacturing Company 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.
← 69423-0675-11 · The 69423-0677-01 · The →
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.