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ARTISTRY STUDiO Rose All Day Anti Acne Toner Pore Refresher SALICYLIC ACID 10 mg/mL Liquid, 200 mL — NDC 10056-0410-00 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ARTISTRY STUDiO Rose All Day Anti Acne Toner Pore Refresher SALICYLIC ACID 10 mg/mL Liquid, 200 mL — NDC 10056-410-00 (Billing 10056-0410-00)

by Access Business Group LLC · 200 mL in 1 BOTTLE

This is a package of 200 mL of ARTISTRY STUDiO Rose All Day Anti Acne Toner Pore Refresher SALICYLIC ACID 10 mg/mL Liquid from Access Business Group LLC, marketed since Sep 2020 and currently FDA-listed. It is this product's only package size.

NDC 10056-0410-00
🏷️ FDA NDC (as labeled) 10056-410-00 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 10056-410-00
Product NDC 10056-410
11-digit billing NDC 10056041000
RxCUI 1047362
UNII O414PZ4LPZ
Application # M006
SPL Set ID a9e26804-7989-41d2-8506-c4b65ca385b7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-09-23
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 1047362
Why two NDCs? The FDA registers this code as 10056-410-00 — 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 → 10056-0410-00. 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.

Clinical

📖 What it is MedlinePlus · NLM

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or b...

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • It is used in a facial routine for acne-prone and oil-prone skin. The routine includes a cleanser, serum, toner and emulsion. Salicylic acid helps loosen and shed dead skin cells.
  • Use the cleanser morning and evening, and the serum in the morning after cleansing. Use the toner in the evening on dry skin, and the emulsion at night after cleansing. Avoid your...
  • Mild stinging, burning, itching, dryness and extra peeling can happen. If dryness or peeling bothers you, try using the serum or toner every other day. If it gets excessive, stop a...
  • It is best not to. Using another topical acne medication at the same time makes irritation and dryness more likely. If you get irritated, use only one at a time.
📖 Read our full Salicylic Acid Topical guide →

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
10056-0410-00 You're viewing this Main listing 200 mL in 1 BOTTLE 2020-09-23 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
ARTISTRY STUDiO Rose All Day Anti Acne Toner Pore Refresher 10 mg/mLthis 10056-0410-00 Access 200 ml — — FDA listed —
Biore 1 g/100g 10596-0199-05 Kao 1 tube — — FDA listed —
NAS Toner 1 g/1001 26052-0042-01 BURT'S 145 liquids — — FDA listed —
Clarifying Toner 1 g/100g 62742-4240-01 Allure 120 g — — FDA listed —
Biome-Balancing Clear and Prevent Acne (Blemish) Treatment Serum 1 g/100mL 70381-0134-02 Murad, 1 bottle — — FDA listed —
Aftaseptic Instant Pain Relief 10 mg/mL 73635-7102-05 Germa 1 bottle — — FDA listed —
Dr. C. Tuna Acne Blemish Control Serum 10 mg/mL 74690-0011-01 Farmasi 1 bottle — — FDA listed —
YOUR Anti Acne Serum .2 g/20mL 84229-0016-00 Skin 20 ml — — Discontinued —
Your Anti-Acne Serum .2 g/20mL 84229-2101-03 Skin 1 ml — — FDA listed —
Wart Remover 1 g/100mL 84302-0001-01 Shenzhen 30 ml — — Discontinued —
Sylvirene Milia Remover 1 g/100mL 85248-0071-01 Jiangxi 40 ml — — FDA listed —
Beilloso FACIAL BUMP REFINING ESSENCE 1 g/100mL 85248-0077-01 Jiangxi 30 ml — — FDA listed —
Serynth Milia Remover 1 g/100mL 85248-0107-01 Jiangxi 30 ml — — FDA listed —
Dermfree Milia Remover 1 g/100mL 85248-0125-01 Jiangxi 30 ml — — FDA listed —
Folupia Milia Remover 1 g/100mL 85248-0147-01 Jiangxi 30 ml — — FDA listed —
Flobow FACIAL BUMP REFINING ESSENCE 1 g/100mL 85248-0168-01 Jiangxi 30 ml — — FDA listed —
Lixuhya MILIA REMOVER ESSENCE 1 g/100mL 85248-0208-01 Jiangxi 40 ml — — FDA listed —
Butterflys tear MILIA REMOVER 1 g/100mL 85248-0213-01 Jiangxi 30 ml — — FDA listed —
Blemish Blitz Emergency Acne Serum .01 g/mL 85779-0003-01 Guangdong 20 ml — — FDA listed —
Milia remover .01 g/mL 87278-0006-01 Guangxi 30 ml — — FDA listed —
Xexlvov Milia Remover 1 g/100mL 87312-0147-01 Shanghai 30 ml — — FDA listed —
Byt Bangytong Milia Remover 1 g/100mL 87382-0107-01 Shenzhen 30 ml — — FDA listed —
Spesolskii Milia Remover Essence 1 g/100mL 87556-0001-01 BEST 30 ml — — FDA listed —
Asterose Wart Remover 1 g/100mL 87786-0003-01 Wenzhou 10 ml — — FDA listed —
Musizlee WART REMOVER 1 g/100mL 87786-0004-01 Wenzhou 10 ml — — FDA listed —
Acne Advanced Cleansing 10 mg/mL 15751-3010-05 Eminence 1 bottle — — FDA listed —
Proactivplus Smoothing BHA Cleanser 10 mg/mL 11410-0216-01 Alchemee, 1 tube — — FDA listed —
Acne Clarifying Cleanser 10 mg/mL 76354-0415-01 e.l.f. 1 bottle — — FDA listed —
Clear Improvement Blackhead Clearing Mask To Scrub 10 mg/mL 59427-0118-01 ORIGINS 75 ml — — FDA listed —
Neutrogena Stubborn Body Acne Cleanser and Exfoliator 10 mg/mL 69968-0759-08 Kenvue 250 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

🏛️
2020
On the market since
Sep 2020
📍
2026
Currently FDA-listed
6 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 S347WMO6M4
    Beta-sitosterol is a plant-derived sterol (waxy substance from vegetable oils and seeds). In medicines, it acts as an emulsifier or thickening agent to help blend oil and water-based ingredients and improve texture.
  • 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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • UNII I835H2IHHX
    A waxy substance derived from plant oils, used as an emulsifier and solubilizer to help mix oil and water ingredients together and keep them blended throughout the product's shelf life.
  • UNII MC2LH51BO7
    A plant-derived oil extracted from chia seeds, used as an emollient and vehicle in topical or oral formulations. It helps deliver active ingredients and may improve product texture or absorption.
  • UNII I670DAL4SZ
    A preservative that fights bacteria and fungi. It keeps medicines and topical products stable and safe from microbial contamination during storage and use.
  • UNII 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • UNII 1Z74184RGV
    Egg phospholipids are naturally derived fats from eggs that help mix oil and water-based ingredients together. They work as emulsifiers in medicines, keeping the formula stable and uniform.
  • UNII 3Q9L08K71N
    Evening primrose oil is a plant-based oil extracted from evening primrose seeds. It's used in medications as an emollient and to improve texture and absorption in soft capsule formulations.
  • UNII X3W0AM1JLX
    A synthetic red dye used to color medicines and products. It helps make pills, liquids, and capsules visually distinct and easier to identify.
  • 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 CA2Y0FE3FX
    A salt derived from licorice root extract, used as a flavoring agent and sweetener. It may also help soothe and protect mucous membranes in throat lozenges and cough products.
  • UNII 2NX48Z0A9G
    Icodextrin is a glucose polymer derived from starch. It acts as a thickening agent and osmotic agent in medicines, helping to control texture and absorption in formulations like eye drops or injectable solutions.
  • UNII D2QHA03458
    A fermented ingredient made by culturing beneficial bacteria in radish root extract. It acts as a natural preservative and humectant, helping keep the product fresh and maintain moisture in the formula.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII 4Y0E651N0F
    A plant-derived emulsifier made from almond oil and polyethylene glycol. It helps mix oil and water-based ingredients together and improves how the medicine dissolves and is absorbed in the body.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII T4L5881Y68
    A plant-derived ingredient from perilla leaves, used as a natural flavoring agent and to provide potential sensory or aromatic qualities to the medicine.
  • UNII 322MS57V7Z
    A plant-derived oil from perilla seeds. It's used as an emollient and skin-conditioning agent to help soften and smooth the product's texture.
  • 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 B697894SGQ
    Polyethylene glycol 400 is a clear, thick liquid made from petroleum-derived polymers. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 56687D1Z4D
    A natural plant extract from pomegranate fruit, used as a flavor and color ingredient to enhance taste and appearance in medicines.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII CS4TE8FF7O
    A plant extract from the petals of the centifolia rose. It's used in medicines as a fragrance, flavoring agent, and for its pleasant scent and taste properties.
  • UNII JWB78P295A
    A plant extract from damask rose flowers used as a natural fragrance, flavoring agent, or coloring component in medicines. It adds pleasant aroma or taste to the product.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 241ATL177A
    Soybean oil is a natural plant oil derived from soybean seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients and improve how the body absorbs them.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII U49SHU1VCI
    A plant extract from common lilac flowers used as a natural flavoring or fragrance agent in medicines to improve taste or aroma.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • 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.

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

The official label also stateswater/aqua, alcohol denat., PEG-8, lactobacillus/punica granatum fruit ferment extract, sodium hydroxide, pentylene glycol, allantoin, ceteth-20, dipotassium glycyrrhizate, disodium EDTA, PEG-60 almond glycerides, butylene glycol, glycerin, maltodextrin, aloe barbadensis leaf juice, dextrin, rosa damascena flower extract, leuconostoc/radish root ferment filtrate, lecithin, syringa vulgaris (lilac) extract, bisabolol, punica granatum fruit extract, phenoxyethanol, rosa centifolia flower extract, salvia hispanica (chia) seed oil, chlorphenesin, red 4 (CI 14700), ceramide NP, beta-sitosterol, perilla ocymoides leaf extract, oenothera biennis (evening primrose) oil, perilla ocymoides seed oil, tocopherol, glycine soja (soybean) oil, potassium sorbate, sodium benzoate, BHT, helianthus annuus (sunflower) seed oil.

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

LabelerAccess Business Group LLC
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code10056
First marketedSep 2020
Product typeHuman Otc Drug
Portfolio15 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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 6 words ▾

Use For the treatment of acne.

⏱️ Dosage and Administration 70 words ▾

Directions Cleanse the skin thoroughly before applying product. Cover the entire affected areas with a thin layer 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/health care practitioner. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

⚠️ Warnings 113 words ▾

Warnings For external use only Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin.

If this occurs, only one product should be used unless directed by a doctor/health care practitioner. Apply to affected areas only Do not use on broken skin or apply to large areas of the body Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Discontinue use if excessive skin irritation develops or increases. If irritation persists, consult a doctor/health care practitioner.

🧪 Active Ingredient 9 words ▾

Active ingredient Salicylic Acid 1.0% (W/W) Purpose Acne Treatment

🧪 Inactive Ingredients 97 words ▾

Inactive ingredients water/aqua, alcohol denat., PEG-8, lactobacillus/punica granatum fruit ferment extract, sodium hydroxide, pentylene glycol, allantoin, ceteth-20, dipotassium glycyrrhizate, disodium EDTA, PEG-60 almond glycerides, butylene glycol, glycerin, maltodextrin, aloe barbadensis leaf juice, dextrin, rosa damascena flower extract, leuconostoc/radish root ferment filtrate, lecithin, syringa vulgaris (lilac) extract, bisabolol, punica granatum fruit extract, phenoxyethanol, rosa centifolia flower extract, salvia hispanica (chia) seed oil, chlorphenesin, red 4 (CI 14700), ceramide NP, beta-sitosterol, perilla ocymoides leaf extract, oenothera biennis (evening primrose) oil, perilla ocymoides seed oil, tocopherol, glycine soja (soybean) oil, potassium sorbate, sodium benzoate, BHT, helianthus annuus (sunflower) seed oil.

🎯 Purpose 3 words ▾

Purpose Acne Treatment

📄 Do Not Use 42 words ▾

Do not use on broken skin or apply to large areas of the body Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Discontinue use if excessive skin irritation develops or increases. If irritation persists, consult a doctor/health care practitioner.

📄 Keep Out of Reach of Children 66 words ▾

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one product should be used unless directed by a doctor/health care practitioner. Apply to affected areas only

📄 Package Label / Principal Display Panel 4 words ▾

Package Labeling: Bottle Bottle2

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

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.

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 ARTISTRY STUDiO Rose All Day Anti Acne Toner Pore Refresher (this brand).

Top reported reactions

Vomiting216
Pruritus205
Weight Decreased188
Condition Aggravated184
Urticaria184
Weight Increased183
Hypertension181

Reporter sex

1,853 reports

Serious outcomes

Death611
Disabling124
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 243 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 Access Business Group LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Access Business Group 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.
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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.