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Proactiv Clean Beginner Bundle Clean Kit Kit — NDC 11410-0229-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Proactiv Clean Beginner Bundle Clean Kit Kit — NDC 11410-229-01 (Billing 11410-0229-01)

by Alchemee, LLC · 1 KIT in 1 BOX * 60 mL in 1 TUBE * 30 mL in 1 TUBE

This is a package of Proactiv Clean Beginner Bundle Clean Kit Kit from Alchemee, LLC, marketed since May 2024 and currently FDA-listed. It is this product's only package size.

NDC 11410-0229-01
🏷️ FDA NDC (as labeled) 11410-229-01 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 →

NDC database record

One package, one record: these facts belong to NDC 11410-229-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
11410 labeler · 229 product · 01 package
Package marketed since
May 8, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 1141022901 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11410-229-01
Product NDC 11410-229
11-digit billing NDC 11410022901
RxCUI 1046894
Application # M006
SPL Set ID 201e1b5e-555a-92c0-e063-6394a90a1360
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-05-08
Dosage form KIT
Quick answers
  • RxCUI (RxNorm): 1046894
Why two NDCs? The FDA registers this code as 11410-229-01 — 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 → 11410-0229-01. 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.

RxNorm drug class

This medicine belongs to the Preparations containing sulfur class.

Drug family (ATC) Preparations containing sulfur
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.

Clinical

🧪 What is this product?

Proactiv Clean Beginner Bundle Clean Kit is an over-the-counter skincare kit marketed under FDA monograph rules. The bundle contains topical cleansing and treatment products that typically include ingredients such as benzoyl peroxide, which is commonly used in acne skincare products to help reduce bacteria and oiliness on the skin. This kit is designed as a starter set for a multi-step skincare routine aimed at managing acne-prone skin.

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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
11410-0229-01 You're viewing this Main listing 1 KIT in 1 BOX * 60 mL in 1 TUBE * 30 mL in 1 TUBE 2024-05-08 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Proactiv Clean Beginner Bundlethis 11410-0229-01 Alchemee, 1 kit — — 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

🏛️
2024
On the market since
May 2024
📍
2026
Currently FDA-listed
2 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.

From the label’s inactive-ingredient sectionWater, Sodium Cocoyl Isethionate, Coco-Glucoside, Acrylates Copolymer, Coconut Acid, Coconut Alcohol, Glycereth-18 Ethylhexanoate, Glycereth-18, Behenyl Alcohol, Titanium Dioxide (CI 77891), Phenoxyethanol, Sodium Isethionate, Sodium Hydroxide, Arachidyl Alcohol, Stearyl Alcohol, Xanthan Gum, Ethylhexylglycerin, Glycerin, Tetrasodium Glutamate Diacetate, Chamomilla Recutita (Matricaria) Flower Extract

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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

LabelerAlchemee, LLC
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code11410
First marketedMay 2024
Product typeHuman Otc Drug
Portfolio26 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.

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 10 words ▾

Mineral Acne Cleanser - Use for the management of acne

⏱️ Dosage and Administration 98 words ▾

Mineral Acne Cleanser - Directions Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs follow the directions stated below. cover the entire affected area with a thin layer and rinse thoroughly one to three times daily because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

⚠️ Warnings 9 words ▾

Mineral Acne Cleanser - Warnings For external use only

🧪 Active Ingredient 8 words ▾

Mineral Acne Cleanser - Active ingredient Sulfur 3%

🧪 Inactive Ingredients 47 words ▾

Mineral Acne Cleanser - Inactive ingredients Water, Sodium Cocoyl Isethionate, Coco-Glucoside, Acrylates Copolymer, Coconut Acid, Coconut Alcohol, Glycereth-18 Ethylhexanoate, Glycereth-18, Behenyl Alcohol, Titanium Dioxide (CI 77891), Phenoxyethanol, Sodium Isethionate, Sodium Hydroxide, Arachidyl Alcohol, Stearyl Alcohol, Xanthan Gum, Ethylhexylglycerin, Glycerin, Tetrasodium Glutamate Diacetate, Chamomilla Recutita (Matricaria) Flower Extract

🎯 Purpose 7 words ▾

Mineral Acne Cleanser - Purpose Acne treatment

📄 Do Not Use 17 words ▾

Mineral Acne Cleanser - Do not use if you on broken skin large areas of the skin

📄 When Using This Product 58 words ▾

Mineral Acne Cleanser - When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. apply only to areas with acne avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

📄 Keep Out of Reach of Children 23 words ▾

Mineral Acne Cleanser - Keep out of reach of children If swallowed, call a Poison Control Center or get medical help right away.

📄 Other Information 14 words ▾

Mineral Acne Cleanser - Other information Store at 20oC – 25oC (68o – 77oF).

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-950-4695

📄 Package Label / Principal Display Panel 45 words ▾

PRINCIPAL DISPLAY PANEL - Proactiv Clean Beginner Breakouts Bundle proactiv® Proactiv Clean Beginner Breakouts Bundle 2-Piece Limited Ulta Exclusive Formulated without parabens, phthalates, cyclic silicones, and sulfates Mineral Acne Cleanser 2 FL. OZ. (60 mL) Azelaic Pore Perfector 1 FL. OZ. (30 mL) image 1

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

About this NDC listing & data coverage

Over-the-counter (OTC) product Kit / multi-component package

Kit / multi-component package

This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.

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 Alchemee, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Alchemee, 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.
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.