NDC 50184-1005-03 — clear days ahead oil-free salicylic acid acne

🆔 Identity & classification

FDA NDC (as labeled) 50184-1005-3

Product NDC 50184-1005

11-digit billing NDC 50184100503

RxCUI 1038982, 1251574

UNII O414PZ4LPZ

Application # M006

SPL Set ID e76dfe48-db23-47e9-8f86-640c9c7bc2a4

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2012-04-11

Route TOPICAL

Dosage form LIQUID

Substance SALICYLIC ACID

Why two NDCs? The FDA registers this code as 50184-1005-3 — 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 → 50184-1005-03. 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.

🏷️ RxNorm drug class

This medicine belongs to the Salicylic acid and derivatives class.

Drug family (ATC) Salicylic acid and derivatives, Other antifungals for topical use, Antiinflammatory agents, non-steroids

Where does this data come from?

Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerPhilosophy Inc.

FDA applicationM006 (OTC MONOGRAPH DRUG)

Labeler code50184

First marketedApr 2012

Product typeHuman Otc Drug

Portfolio3 products on file

🔎 All NDCs from Philosophy Inc.

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

📗 Our plain-language guide HelloPharmacist

It's designed to treat acne. Salicylic acid helps by loosening and removing dead skin cells that clog pores — the buildup that leads to breakouts. The multi-step system on this lab...
What is this salicylic acid product actually supposed to do for my skin?
Some mild tingling, stinging, and peeling is actually expected — that's the salicylic acid doing its job by clearing away dead skin cells. But if the burning or peeling feels exces...
My skin feels like it's burning and peeling. Is that normal?

📖 Read our full Salicylic Acid Topical guide →

Patient education

📘 MedlinePlus patient leaflet ↗

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.

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.

💲 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 system	Per mL	Per 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.

Try another pack size: 240 ml 240 ml

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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Proactivplus Smoothing BHA Cleanser 10 mg/mL 11410-0216-01	Alchemee,	1 tube	—	—	FDA listed	—
Acne Advanced Cleansing 10 mg/mL 15751-3010-05	Eminence	1 bottle	—	—	FDA listed	—
Nas Pore Refining Scrub 1 g/100g 26052-0040-01	BURT'S	110 g	—	—	FDA listed	—
blackhead solutions 7 day deep pore cleanse and scrub acne medication 10 mg/mL 49527-0062-02	CLINIQUE	1 tube	—	—	Discontinued	—
clear days ahead oil-free salicylic acid acne treatment cleanser 2.4 g/240mLthis 50184-1005-03	Philosophy	90 ml	—	—	FDA listed	—
Sei Bella Clarity Clear Refining Foaming Cleanser Acne treatment 1.8 g/180mL 54473-0401-01	Melaleuca,	180 ml	—	—	FDA listed	—
Acne wash facial cleanser pink grapefruit 2 g/200mL 57337-0080-01	Rejoice	200 ml	—	—	FDA listed	—
Acne wash facial cleanser Tea tree oil 2 g/200mL 57337-0081-01	Rejoice	200 ml	—	—	FDA listed	—
Clear Improvement Blackhead Clearing Mask To Scrub 10 mg/mL 59427-0118-01	ORIGINS	75 ml	—	—	FDA listed	—
Dove 1 g/100mL 64942-2074-01	CONOPCO	512 ml	—	—	FDA listed	—
Dove 1 g/100mL 64942-2093-01	CONOPCO	500 ml	—	—	Discontinued	—
Neutrogena Stubborn Texture Daily Cleanser 10 mg/mL 69968-0704-06	Kenvue	186 ml	—	—	FDA listed	—
Neutrogena Stubborn Body Acne Cleanser and Exfoliator 10 mg/mL 69968-0759-08	Kenvue	250 ml	—	—	FDA listed	—
NAELI Exfoliator AHA-BHA Face Cleanser 10 mg/mL 73670-0606-00	ALLI	1 bottle	—	—	FDA listed	—
NAELI Exfoliator AHA BHA Face Cleanser 10 mg/mL 73670-0620-00	ALLI	1 bottle	—	—	FDA listed	—
Acne Clarifying Cleanser 10 mg/mL 76354-0415-01	e.l.f.	1 bottle	—	—	FDA listed	—
Acne Wash 1 mg/100mg 82442-0805-01	Target	650 mg	—	—	FDA listed	—
bareMinerals Blemish Remedy Acne Treatment Gelee Cleanser 10 mg/g 98132-0770-01	Orveon	1 tube	—	—	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

🏛️

2012

On the market since

Apr 2012

📍

2026

Currently FDA-listed

14 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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Salicylic Acid (matched by generic name) — the program that covers self-administered drugs. 2 manufacturers.

⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Salicylic Acid. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.

Period

Total Part D spend

$11.2K

Claims incl. refills

43

Beneficiaries

35

Spend / beneficiary

$319.01

Spend / claim

$259.66

Trend by period

💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
50184-1005-01	240 mL in 1 BOX (50184-1005-1)	2012-04-11	Active
50184-1005-02	240 mL in 1 BOTTLE (50184-1005-2)	2012-04-11	Active
50184-1005-03 You're viewing this	90 mL in 1 BOTTLE (50184-1005-3)	2012-04-11	Active

Pack size FAQ

What quantity is in NDC 50184-1005-03?

NDC 50184-1005-03 contains 90 mL — 90 ml in 1 bottle.

What is the difference between NDC 50184-1005-03 and NDC 50184-1005-01?

Both are clear days ahead oil-free salicylic acid acne treatment cleanser 2.4 g/240mL Liquid — the drug itself is identical. NDC 50184-1005-03 is the 90 mL package, while NDC 50184-1005-01 is the 240 ml package.

What NDC number is used to bill for this package of clear days ahead oil-free salicylic acid acne treatment cleanser 2.4 g/240mL Liquid?

Bill NDC 50184-1005-03 — the 11-digit billing format is 50184100503. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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)	— 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.

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 50184-1005-3, 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: 50184-1005-03, written without dashes as 50184100503. 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 50184-1005-03, the first segment (50184) is the labeler code FDA assigned to Philosophy Inc.; the middle segment (1005) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) 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 Philosophy Inc.. Listing status can change — the directory data on this page refreshes weekly.

Does this product come in other package sizes?

Yes — the FDA directory lists 2 other package presentations of this same product, including 240 ml (50184-1005-01), 240 ml (50184-1005-02). Each has its own NDC and its own page — see the package list near the top of this page.

Who lists this product with the FDA?

Philosophy 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 6 words ▾

Indications For the treatment of acne

⏱️ Dosage and Administration 33 words ▾

Directions apply to slightly damp face, and massage for 30-60 seconds. rinse thoroughly. use morning and evening. if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

⚠️ Warnings 88 words ▾

Warnings For external use only Ask a doctor or pharmacist before using if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient Salicylic Acid (1.0%)

🧪 Inactive Ingredients 49 words ▾

Inactive ingredients water, sodium c14-16 olefin sulfonate, acrylates crosspolymer-4, cocamidopropyl betaine, polysorbate 20, niacinamide, glycerin, panthenol, citrus aurantium dulcis (orange) peel extract, hydrolyzed jojoba esters, jojoba esters, disodium capryloyl glutamate, sodium chloride, sodium sulfate, potassium chloride, butylene glycol, citric acid, sodium hydroxide, hydrogen peroxide, propylene glycol, methylchloroisothiazolinone, methylisothiazolinone, o-cymen-5-ol.

🎯 Purpose 3 words ▾

Purpose Acne Treatment

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

🔗 Related NDC lookups

🧪 All Salicylic Acid NDCsSame ingredient 🏭 All Philosophy labeler NDCsLabeler code 50184 📖 Read the Salicylic Acid drug informationUses, warnings & side effects

clear days ahead oil-free salicylic acid acne treatment cleanser 2.4 g/240mL Liquid, 90 mL

🆔 Identity & classification

🏷️ RxNorm drug class

🏭 Manufacturer & labeler

🩺 Clinical

Patient education

Supplement & herbal interactions

🧪 Inactive Ingredients / Excipients

Inactive ingredient FAQ

💲 Pricing

🔁 Therapeutic equivalents

⏳ Availability & generic status

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

📦 Packaging — all sizes for this product

Pack size FAQ

🧭 About this NDC listing & data coverage

Questions about this listing

📄 FDA label — Drug Facts FDA SPL

🔗 Related NDC lookups