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SUNDAY RILEY U.F.O Acne Treatment Face Oil Salicylic Acid 15 mg/mL Oil — NDC 73001-0460-35 package photo

SUNDAY RILEY U.F.O Acne Treatment Face Oil Salicylic Acid 15 mg/mL Oil

by Sunday Riley Modern Skincare, LLC · 1 BOTTLE, GLASS in 1 BOX (73001-460-35) / 35 mL in 1 BOTTLE, GLASS
NDC 73001-0460-35
🏷️ FDA NDC (as labeled) 73001-460-35 billing pads the product segment with a zero
This package
Contains35 mL in 1 bottle, glass Pack sizes3 compare ↓
Also comes in: 5 mL 73001-0460-05 15 mL 73001-0460-15
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 73001-460-35
Product NDC 73001-460
11-digit billing NDC 73001046035
RxCUI 2170987
UNII O414PZ4LPZ
Application # M006
SPL Set ID 90bd3b3b-3b42-4369-8b9a-a81dd8b6a1e5
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-04-30
Route TOPICAL
Dosage form OIL
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 73001-460-35 — 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 → 73001-0460-35. 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

LabelerSunday Riley Modern Skincare, LLC
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code73001
First marketedApr 2017
Product typeHuman Otc Drug
Portfolio3 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.

🩺 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'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 →

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII L65MV77ZG6
    A naturally occurring alcohol compound derived from plants, used as a fragrance and flavoring agent in medicines to improve taste and smell.
  • UNII 575DY8C1ER
    Aloe vera flower is a natural plant extract used in medicines as a skin-soothing agent and emollient. It helps soften and moisturize formulations, particularly in topical products like creams and lotions.
  • UNII 70J9Z0J26P
    A natural resin from tree sap, amber is used as a colorant and flavor component in some medicines. It gives products a warm, golden appearance and mild aromatic qualities.
  • UNII 54JB35T06A
    A natural oil extracted from apricot pits, used as an emollient and lubricant in topical products. It helps soften the skin and improves the texture and spreadability of creams and lotions.
  • UNII 3TE8A92UPM
    Azadirachta indica flower is a botanical extract from the neem plant. It may be used in formulations for its traditional preservative or antioxidant properties to help maintain product stability.
  • UNII HKY915780T
    A plant extract from the neem tree, used as a natural flavoring agent and preservative in medicines. It may help maintain product stability and add bitter taste characteristics.
  • UNII 60F80Z61A9
    A fragrant plant oil extracted from chamomile flowers. It's used as a flavoring agent and fragrance in medicines to improve taste and smell, making the product more pleasant to take.
  • UNII D4BGE91OXH
    An aromatic oil extracted from bitter orange blossoms, used as a flavoring agent and fragrance in medicines to mask unpleasant tastes and improve palatability.
  • UNII VLJ6WOT3K5
    A plant extract from the Coccinia indica fruit, used in herbal and traditional formulations. It may serve as a natural flavoring agent, colorant, or active botanical component depending on the product's intended use.
  • UNII 4004498D06
    A red algae extract used as a natural colorant and pH buffer in medicines. It provides reddish tones to tablets and capsules while helping maintain stable acidity levels in the formulation.
  • UNII 73KDS3BW5E
    A plant oil extracted from cranberry seeds, used in medications as an emollient and emulsifier. It helps blend oil and water-based ingredients together and keeps the product's texture smooth and stable.
  • UNII AKP926H71P
    A plant-derived oil extracted from cucumber seeds, used primarily as an emollient and skin-conditioning agent. It helps soften and smooth the product's texture while providing moisturizing properties to topical formulations.
  • UNII H2HC4RY52C
    A natural extract from turmeric plant leaves, used as a colorant and flavoring agent to add color and taste to the medicine.
  • UNII J8T3X564IH
    A clear oily liquid derived from sebacic acid, used as a plasticizer and solvent in pharmaceutical coatings and films to improve flexibility and help active ingredients dissolve properly.
  • UNII SA6A6V432S
    Dimethyl isosorbide is a clear liquid solvent derived from natural sugar sources. It helps dissolve active ingredients and improve their absorption in liquid medicines and topical products.
  • UNII W5K7RAS4VK
    A purple vegetable extract used as a natural colorant in some medicines. It provides color to tablets or capsules without affecting how the drug works.
  • UNII MJ2YTT4J8M
    Ethyl linoleate is a fatty acid ester derived from linoleic acid. It acts as an emollient and solvent in formulations, helping to dissolve or carry active ingredients and improve product texture and absorption.
  • UNII 2788Z9758H
    A plant extract from licorice root used as a sweetener, flavoring agent, and natural emulsifier in medicines. It helps improve taste and may aid in keeping ingredients evenly mixed throughout the product.
  • UNII YR377U58W9
    Grapefruit oil is a natural aromatic extract from grapefruit peel. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance component.
  • UNII R9QTB5E82N
    Hexylresorcinol is a chemical compound used in medicines as an antimicrobial preservative and antiseptic agent. It helps prevent bacterial growth and keeps the product stable during storage.
  • UNII SCJ765569P
    Holy basil leaf is a plant-derived ingredient used in some formulations as a flavoring agent or botanical additive. It may contribute taste and aroma to the medicine.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII 84XB4DV00W
    Linseed oil is a plant-based oil extracted from flax seeds. It's used in medicines as an emollient and lubricant to improve texture and help with ingredient mixing in formulations.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII REM6A5QMC0
    A plant-based oil extracted from moringa tree seeds. It's used in medicines as an emollient to soften and smooth the product, and sometimes as a natural carrier or conditioning agent in formulations.
  • UNII CS4U38E731
    A plant-derived oil from nigella sativa seeds, used as a carrier and emollient in formulations. It helps dissolve or suspend active ingredients and improves product texture and absorption.
  • UNII 7SAB275FP2
    A plant extract made from basil flowers and leaves. It's used in medicines as a flavoring agent and may help preserve the product by providing natural antimicrobial properties.
  • UNII 0UI45XV0T6
    A plant oil extracted from pomegranate seeds. It's used in formulations as an emollient to soften and smooth the product texture, and sometimes as a carrier or conditioning agent in topical preparations.
  • UNII IJ67X351P9
    A natural plant extract from rosemary leaves used as a preservative to help prevent oils and fats in the medicine from spoiling or becoming rancid during storage.
  • UNII NYY23HEN06
    A plant oil extracted from milk thistle seeds, used as an emollient and carrier to improve texture and help distribute active ingredients evenly throughout the formulation.
  • 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 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 856YO1Z64F
    Turmeric is a natural spice derived from the turmeric plant root. It serves as a colorant in medicines, giving products a yellow or golden appearance, and may also provide mild flavoring.

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

The official label also statesSilybum Marianum (Milk Thistle) Seed Oil, Nigella Sativa (Black Cumin) Seed Oil, Cucumis Sativus (Cucumber) Seed Oil, Punica Granatum (Pomegranate) Seed Oil, Diisopropyl Sebacate, Vaccinium Macrocarpon (Cranberry) Seed Oil, Dimethyl Isosorbide, Linum Usitatissimum (Flax) Seed Oil, Caprylic/Capric Triglyceride, Glycyrrhiza Glabra (Licorice) Root Extract, Prunus Armeniaca (Apricot) Kernel Oil, Hexylresorcinol, Ethyl Linoleate, Melia Azadirachta Leaf Extract, Chamomilla Recutita (Matricaria) Flower Oil, Citrus Aurantium Amara (Bitter Orange) Flower Oil, Melia Azadirachta Flower Extract, Helianthus Annuus (Sunflower) Seed Oil, 4-Terpineol, Simmondsia Chinensis (Jojoba) Seed Oil, Coccinia Indica Fruit Extract, Solanum Melongena (Eggplant) Fruit Extract, Amber Powder, Curcuma Longa (Turmeric) Root Extract, Curcuma Longa (Turmeric) Leaf Extract, Ocimum Sanctum Leaf Extract, Aloe Barbadensis Flower Extract, Corallina Officinalis Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Moringa Oleifera Seed Oil, Tocopherol, Citrus Paradisi (Grapefruit) Peel Oil, Ocimum Basilicum (Basil) Flower/Leaf Extract.

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.

💲 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.
Try another pack size: 5 mL 15 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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
SUNDAY RILEY U.F.O Acne Treatment Face Oil 15 mg/mLthis 73001-0460-35 Sunday 1 bottle — — FDA listed —
Kiehls Since 1851 Blue Herbal Acne Cleanser Treatment with Frankincense and Ginger Root 15 mg/mL 49967-0086-01 L'Oreal 75 ml — — FDA listed —
Kiehls Since 1851 Blue Herbal Acne Cleanser Treatment 15 mg/mL 49967-0618-01 L'Oreal 75 ml — — FDA listed —
Kiehls Since 1851 Dermatologist Solutions Breakout Control Acne Treatment Facial 15 mg/mL 49967-0875-02 L'Oreal 5 ml — — FDA listed —
Clear Improvement Acne Clearing Hydrating Ltn 15 mg/mL 59427-0117-01 ORIGINS 1 bottle — — FDA listed —
SkinCeuticals Blemish Plus Age Defense Acne Treatment 15 mg/mL 82046-0558-01 LOreal 1 bottle — — FDA listed —
Proactiv Blemish Control Body Cream 15 mg/mL 11410-0214-01 Alchemee, 1 tube — — FDA listed —
Thayers Natural Remedies Since 1847 Blemish Clearing Cleanser 15 mg/mL 49967-0070-01 LOreal 132 ml — — FDA listed —
Byoma Acne Control Moisturizer 15 mg/mL 84821-0006-01 Byoma 50 ml — — FDA listed —
Super Spot Remover Acne Treatment 15 mg/mL 59427-0005-01 ORIGINS 10 ml — — FDA listed —
SkinCeuticals Blemish Plus Age Defense Acne Treatment 15 mg/mL 49967-0097-05 L'Oreal 1 bottle — — 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

🏛️
2017
On the market since
Apr 2017
📍
2026
Currently FDA-listed
9 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.

🔬 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 Salicylic Acid — the ingredient across all brands.

Top reported reactions

Dry Skin12,766
Erythema12,318
Acne11,763
Skin Burning Sensation11,557
Skin Irritation7,730
Skin Exfoliation5,759
Rash4,766

Age at onset

Neonate7
Infant1
Child16
Adolescent30
Adult334
Elderly131

Reporter sex

52,595 reports
Male · 27%
Female · 73%
Unknown · 0%

Serious outcomes

Hospitalization800
Death632
Life-threatening214
Disabling147
Reports over time (by year) — tap or hover for the count & year
2024 2025 2026 907 111
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
73001-0460-05 1 BOTTLE in 1 BOX (73001-460-05) / 5 mL in 1 BOTTLE 2017-04-30 Active
73001-0460-15 1 BOTTLE in 1 BOX (73001-460-15) / 15 mL in 1 BOTTLE 2017-04-30 Active
73001-0460-35 You're viewing this 1 BOTTLE, GLASS in 1 BOX (73001-460-35) / 35 mL in 1 BOTTLE, GLASS 2024-12-26 Active

Pack size FAQ

What quantity is in NDC 73001-0460-35?
NDC 73001-0460-35 is listed by the FDA — 1 bottle, glass in 1 box / 35 ml in 1 bottle, glass.
What NDC number is used to bill for this package of SUNDAY RILEY U.F.O Acne Treatment Face Oil Salicylic Acid 15 mg/mL Oil?
Bill NDC 73001-0460-35 — the 11-digit billing format is 73001046035. 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) ✓ 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 73001-460-35, 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: 73001-0460-35, written without dashes as 73001046035. 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 73001-0460-35, the first segment (73001) is the labeler code FDA assigned to Sunday Riley Modern Skincare, LLC; the middle segment (0460) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (35) 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 Sunday Riley Modern Skincare, LLC. 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 1 bottle (73001-0460-05), 1 bottle (73001-0460-15). 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?
Sunday Riley Modern Skincare, 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.

📄 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 23 words ▾

Uses • For the management of acne • Penetrates pores to control blackheads • Helps prevent new acne blemishes and blackheads from forming

⏱️ Dosage and Administration 70 words ▾

Directions • Cleanse the skin thoroughly before applying medication. • Cover the entire affected area with a thin layer 1 to 3 times daily. • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a doctor. • If bothersome dryness occurs, reduce application to once a day or every other day.

⚠️ Warnings 68 words ▾

Warnings For external use only. When using this product • Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. • If this occurs, only one medication should be used unless directed by a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active Ingredients Salicylic Acid 1.5%

🧪 Inactive Ingredients 136 words ▾

Inactive Ingredients Silybum Marianum (Milk Thistle) Seed Oil, Nigella Sativa (Black Cumin) Seed Oil, Cucumis Sativus (Cucumber) Seed Oil, Punica Granatum (Pomegranate) Seed Oil, Diisopropyl Sebacate, Vaccinium Macrocarpon (Cranberry) Seed Oil, Dimethyl Isosorbide, Linum Usitatissimum (Flax) Seed Oil, Caprylic/Capric Triglyceride, Glycyrrhiza Glabra (Licorice) Root Extract, Prunus Armeniaca (Apricot) Kernel Oil, Hexylresorcinol, Ethyl Linoleate, Melia Azadirachta Leaf Extract, Chamomilla Recutita (Matricaria) Flower Oil, Citrus Aurantium Amara (Bitter Orange) Flower Oil, Melia Azadirachta Flower Extract, Helianthus Annuus (Sunflower) Seed Oil, 4-Terpineol, Simmondsia Chinensis (Jojoba) Seed Oil, Coccinia Indica Fruit Extract, Solanum Melongena (Eggplant) Fruit Extract, Amber Powder, Curcuma Longa (Turmeric) Root Extract, Curcuma Longa (Turmeric) Leaf Extract, Ocimum Sanctum Leaf Extract, Aloe Barbadensis Flower Extract, Corallina Officinalis Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Moringa Oleifera Seed Oil, Tocopherol, Citrus Paradisi (Grapefruit) Peel Oil, Ocimum Basilicum (Basil) Flower/Leaf Extract.

🎯 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 ↗
← 73001-0305-15 · Sunday 73001-0505-01 · Sunday →
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.