NDC 81515-0540-00 — Peach Slices 3 Step Acne Starter Kit SALICYLIC ACID

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 81515-540-00

Product NDC 81515-540

11-digit billing NDC 81515054000

RxCUI 248684, 251577, 562600

UPC 0818000022751

Application # M006

SPL Set ID 0c8860ca-5376-4e98-a7a9-4668dff4f0aa

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2024-08-14

Dosage form KIT

Quick answers

RxCUI (RxNorm): 248684

Why two NDCs? The FDA registers this code as 81515-540-00 — 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 → 81515-0540-00. 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.

FDA openFDA NDC Directory · synced Oct 1, 2026
FDA label on DailyMed · label index refreshed Oct 6, 2026
RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
Medi-Span GPI (licensed)
First Databank (licensed) · refreshed Oct 1, 2026

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.

RxClass (NLM) · catalog refreshed Oct 1, 2026

Clinical

🧪 What is this product?

This is an over-the-counter acne starter kit containing salicylic acid, a topical ingredient commonly used in skincare products designed to help manage acne-prone skin. Salicylic acid functions as a keratolytic agent, meaning it is typically used to help break down and remove dead skin cells and reduce excess oil buildup in pores. This kit is marketed as an OTC monograph drug product under FDA regulations for acne treatment preparations.

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.

MedlinePlus (NLM) · refreshed Oct 1, 2026
FDA label on DailyMed · label index refreshed Oct 6, 2026

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 each	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.

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.

CMS NADAC weekly file
CMS ASP pricing files · refreshed Sep 20, 2026
CMS Medicaid State Drug Utilization Data · refreshed Oct 6, 2026
CMS Part D plan pricing files · refreshed Sep 24, 2026
VA National Acquisition Center price file

Packaging — all sizes for this product

Package NDC	Description	Marketing start	Marketing end	Status
81515-0540-00 You're viewing this Main listing	1 KIT in 1 KIT * 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE * 1 TUBE in 1 CARTON / 30 mL in 1 TUBE * 1 TUBE in 1 CARTON / 30 mL in 1 TUBE	2024-08-14	—	Active

Therapeutic equivalents

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Salicylicum acidum 6 [hp_C]/6[hp_C] 00220-4526-41	Boiron	1 tube	—	—	FDA listed	—
Salicylicum acidum 30 [hp_C]/30[hp_C] 00220-4528-41	Boiron	1 tube	—	—	FDA listed	—
Acne Advanced Treatment System 15751-3000-03	Eminence	1 kit	—	—	FDA listed	—
Compound W Total Care Wart and Skin Kit 49354-0130-00	HK	1 kit	—	—	FDA listed	—
Dr. C. Tuna Acne Clear Complexion Cleanser 74690-0021-00	Farmasi	1 kit	—	—	FDA listed	—
Ambi Even and Clean Skin Tone Kit 73453-0110-01	Ambi	1 kit	—	—	FDA listed	—
Neutrogena Evenly Clear Acne Prone Skin Essentials 69968-1005-09	Kenvue	1 kit	—	—	FDA listed	—
Salicylicum Acidum 200 [kp_C]/200[kp_C] 00220-4512-41	Boiron	1 tube	—	—	FDA listed	—
Peach Slices 3 Step Acne Starter Kitthis 81515-0540-00	Peach	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.

FDA openFDA NDC Directory · synced Oct 1, 2026
FDA Orange Book · refreshed Oct 3, 2026
CMS NADAC weekly file

Availability & generic status

🏛️

2024

On the market since

Aug 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.

FDA Orange Book · refreshed Oct 3, 2026

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 (Aqua), Glycerin, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Betaine, Sodium Chloride, Cucumis Sativus (Cucumber) Fruit Water, Sodium Hyaluronate, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Sodium Benzoate, Butylene Glycol, Potassium Sorbate, Caprylyl Glycol, 1,2-Hexanediol, Sodium Hydroxide, Citric Acid, Ethylhexylglycerin, Phenoxyethanol Water (Aqua), Butylene Glycol, Arginine, Allantoin, Cucumis Sativus (Cucumber) Fruit Water, Glycerin, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Lactic Acid, Glycolic Acid, Potassium Sorbate, Sodium Benzoate, Citric Acid Water (Aqua), Caprylic/Capric Triglyceride, Propanediol, Butylene Glycol, Cetyl Ethylhexanoate, Ethoxydiglycol, Glyceryl Stearate, 1,2-Hexanediol, Cetearyl Alcohol, Cucumis Sativus (Cucumber) Fruit Water, Centella Asiatica Extract, Sodium Acetylated Hyaluronate, Sodium Hydrolyzed Crosspolymer, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate, Sclerotium Gum, Malpighia Emarginata (Acerola) Fruit Extract, Glycerin, Allantoin, Sodium Benzoate, Potassium Sorbate, Potassium Hydroxide, Sodium Phytate, Niacinamide, Polyacrylate Crosspolymer-6, Citric Acid, Ethylhexylglycerin, T-Butyl Alcohol, Pentylene GLycol, Sodium Polyacrylate

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.

FDA label on DailyMed · label index refreshed Oct 6, 2026
FDA openFDA NDC Directory · synced Oct 1, 2026

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

LabelerPeach & Lily, Inc

FDA applicationM006 (OTC MONOGRAPH DRUG)

Labeler code81515

First marketedAug 2024

Product typeHuman Otc Drug

More NDCs from Peach & Lily, Inc labeler code 81515

🔎 All NDCs from Peach & Lily, 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.

FDA openFDA NDC Directory · synced Oct 1, 2026
Drugs@FDA

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 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel

🎯 Indications and Usage 18 words ▾

Use: For the treatment of acne

⏱️ Dosage and Administration ~1 min read ▾

Directions: Wet face. Dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area. Cover the entire affected area with a thin layer and rinse thoroughly with warm water 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.

Directions: Cleanse skin thoroughly before applying this product. Cover the entire affected area 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. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

⚠️ Warnings ~2 min read ▾

Warnings: For external use only. 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.

Avoid contact with eyes. If contact occurs, flush thoroughly with water. Sun Alert: Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings: For external use only. 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 the same time.

If irritation occurs, only use one topical medication at a time. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing, and limit sun exposure while using this product and for a week afterward. Keep out of reach of children.

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

Warnings: For external use only. 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 the same time.

If irritation occurs, only use one topical medication at a time. Avoid contact with eyes. If contact occurs, flush thoroughly with water Sun Alert: Because this product may make your skin more sensitive to the sun, be certain you have adequate sunscreen protection while using this product and for a week after you discontinue use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 24 words ▾

Active ingredient Salicylic Acid 2% Purpose Acne medication

Active ingredient Salicylic Acid 0.5% Purpose Acne medication

🧪 Inactive Ingredients 141 words ▾

Inactive Ingredients: Water (Aqua), Glycerin, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Betaine, Sodium Chloride, Cucumis Sativus (Cucumber) Fruit Water, Sodium Hyaluronate, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Sodium Benzoate, Butylene Glycol, Potassium Sorbate, Caprylyl Glycol, 1,2-Hexanediol, Sodium Hydroxide, Citric Acid, Ethylhexylglycerin, Phenoxyethanol

Inactive Ingredients: Water (Aqua), Butylene Glycol, Arginine, Allantoin, Cucumis Sativus (Cucumber) Fruit Water, Glycerin, Centella Asiatica Extract, Malpighia Emarginata (Acerola) Fruit Extract, Lactic Acid, Glycolic Acid, Potassium Sorbate, Sodium Benzoate, Citric Acid

Inactive Ingredients: Water (Aqua), Caprylic/Capric Triglyceride, Propanediol, Butylene Glycol, Cetyl Ethylhexanoate, Ethoxydiglycol, Glyceryl Stearate, 1,2-Hexanediol, Cetearyl Alcohol, Cucumis Sativus (Cucumber) Fruit Water, Centella Asiatica Extract, Sodium Acetylated Hyaluronate, Sodium Hydrolyzed Crosspolymer, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate, Sclerotium Gum, Malpighia Emarginata (Acerola) Fruit Extract, Glycerin, Allantoin, Sodium Benzoate, Potassium Sorbate, Potassium Hydroxide, Sodium Phytate, Niacinamide, Polyacrylate Crosspolymer-6, Citric Acid, Ethylhexylglycerin, T-Butyl Alcohol, Pentylene GLycol, Sodium Polyacrylate

🎯 Purpose 9 words ▾

Purpose Acne medication

📄 When Using This Product 165 words ▾

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. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

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 the same time. If irritation occurs, only use one topical medication at a time. Avoid contact with eyes. If contact occurs, flush thoroughly with water.

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 the same time. If irritation occurs, only use one topical medication at a time. Avoid contact with eyes. If contact occurs, flush thoroughly with water

📄 Keep Out of Reach of Children 57 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 12 words ▾

Questions or Comments? 1-866-519-4752

📄 Package Label / Principal Display Panel 24 words ▾

Package Labelling: Kit (81515-540-00) Kit.jpg

Package Labelling: 81515-541-01 Acne Clarifying.jpg Acne Clarifying2.jpg

Package Labelling: 81515-542-01 Acne Exfoliating.jpg

Package Labelling: 81515-543-01 Acne Oil.jpg Acne Oil2.jpg

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.

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 Peach & Lily, Inc. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

Peach & Lily, 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.

Related NDC lookups

🧪 All Salicylic Acid NDCsSame ingredient 🏭 All Peach labeler NDCsLabeler code 81515 📖 Read the Salicylic Acid drug informationUses, warnings & side effects

Peach Slices 3 Step Acne Starter Kit SALICYLIC ACID Kit — NDC 81515-540-00 (Billing 81515-0540-00)

NDC database record

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

RxNorm drug class

Clinical

Patient education

Supplement & herbal interactions

Pricing

Packaging — all sizes for this product

Therapeutic equivalents

Availability & generic status

Inactive Ingredients / Excipients

Inactive ingredient FAQ

Manufacturer & labeler

More NDCs from Peach & Lily, Inc labeler code 81515

FDA label — Drug Facts FDA SPL

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

About this NDC listing & data coverage

Kit / multi-component package

Questions about this listing