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e.l.f Plz Clarify Facial Oil 2 g/100mL Liquid, 30 mL — NDC 70412-0401-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

e.l.f Plz Clarify Facial Oil 2 g/100mL Liquid, 30 mL — NDC 70412-401-01 (Billing 70412-0401-01)

by Zhejiang Ayan Biotech Co., Ltd. · 30 mL in 1 BOTTLE, GLASS

This is a package of 30 mL of e.l.f Plz Clarify Facial Oil 2 g/100mL Liquid from Zhejiang Ayan Biotech Co., Ltd., marketed since Nov 2024 and currently FDA-listed. It is this product's only package size.

NDC 70412-0401-01
🏷️ FDA NDC (as labeled) 70412-401-01 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 70412-401-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70412 labeler · 401 product · 01 package
Package marketed since
Nov 30, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7041240101 7
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70412-401-01
Product NDC 70412-401
11-digit billing NDC 70412040101
RxCUI 251577
UNII O414PZ4LPZ
Application # M006
SPL Set ID 25a8a0fe-d09b-3e20-e063-6394a90a51f0
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-11-30
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 251577
Why two NDCs? The FDA registers this code as 70412-401-01 — 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 → 70412-0401-01. 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 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
70412-0401-01 You're viewing this Main listing 30 mL in 1 BOTTLE, GLASS 2024-11-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PanOxyl Clarifying Exfoliant 2 g/100mL 00316-0296-04 Crown 118 ml — — FDA listed —
Hero Pore Release Blackhead Clearing 20 mg/mL 10237-0001-00 Church 100 ml — — FDA listed —
Sulfur 8 Anti-Dandruff Braid 20 mg/mL 12022-0021-00 J. 356 ml — — FDA listed —
Sulfur 8 Fresh Anti-Dandruff 20 mg/mL 12022-0028-00 J. 355 ml — — FDA listed —
Kiehls Since 1851 Dermatologist Solutions Truly Targeted Acne Clearing Solution 20 mg/mL 49967-0055-01 L'Oreal 1 bottle — — FDA listed —
Thayers Since 1847 Natural Remedies Double Action Acne Serum 20 mg/mL 49967-0062-01 L'Oreal 1 bottle — — FDA listed —
Thayers Since 1847 Natural Remedies Blemish Clearing Witch Hazel Aloe Vera Formula Toner 20 mg/mL 49967-0523-01 L'Oreal 355 ml — — FDA listed —
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 51150-0995-01 SICOS 1 bottle — — FDA listed —
Dr. Gross AB Acne Daily Breakout 20 mg/mL 51326-0179-01 Topiderm, 1 bottle — — FDA listed —
Clear Proof Blemish Control Toner Acne Medication 2 g/100mL 51531-6743-05 Mary 1 bottle — — FDA listed —
Anti-Everything Face Serum 2 g/100mL 54111-0180-01 Bentley 1 bottle — — FDA listed —
Emuaid 2 g/100mL 55926-0029-01 Speer 30 ml — — FDA listed —
Exuviance Daily Acne Peel 20 mg/mL 58414-0017-02 NeoStrata 1 bottle — — FDA listed —
Atrix Clarifying Toner 20 mg/mL 59088-0444-08 PureTek 118 ml — — FDA listed —
Acne Warrior Clearing Astringent 2 g/100mL 61197-0121-00 Pacifica 236 ml — — FDA listed —
Clenziderm Pore Therapy Acne Treatment 20 mg/mL 62032-0612-04 Obagi 148 ml — — FDA listed —
Acne Oil Control Primer 20 mg/g 62742-4211-02 Allure 1 tube — — FDA listed —
Shea Moisture 2 g/100mL 64942-2355-02 Conopco 1 bottle — — FDA listed —
Jack Black Bump Fix 20 g/1000g 66738-0022-01 Jack 183 g — — FDA listed —
Pharma Clear Spot Treatment 2 g/100mL 67879-0104-51 PHARMAGEL 1 tube — — FDA listed —
AGE Bright Clearing Serum 20 mg/mL 68479-0184-00 Dermalogica, 3 ml — — FDA listed —
Breakout Clearing Booster 2 mg/100mL 68479-0772-00 Dermalogica, 2 ml — — FDA listed —
Breakout Clearing Booster 2 g/100mL 68479-0773-02 Dermalogica, 1 bottle — — FDA listed —
Neutrogena Clear Pore Oil-Eliminating Astringent 20 mg/mL 69968-0028-08 Kenvue 236 ml — — FDA listed —
Clean and Clear Essentials Deep Cleaning Astringent 20 mg/mL 69968-0209-08 Kenvue 240 ml — — FDA listed —
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0521-08 Kenvue 237 ml — — FDA listed —
Clean and Clear Essentials Acne Toner 20 mg/mL 69968-0820-08 Kenvue 240 ml — — FDA listed —
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0925-08 Kenvue 236 ml — — FDA listed —
Acne Spot Treatment 20 mg/mL 70060-1505-01 CosMedical 9 ml — — FDA listed —
e.l.f Plz Clarify Facial Oil 2 g/100mLthis 70412-0401-01 Zhejiang 30 ml — — FDA listed —
Exfo Tonic Acne Treatment 2 g/100mL 70764-0104-51 CONTROL 1 bottle — — FDA listed —
L BRI Pure n Natural Deep Clean Toner 20 mg/mL 71238-0218-00 L'BRI 188 ml — — FDA listed —
Viaderma Clear Acne Treatment 20 mg/mL 71262-0017-15 VIADERMA 1 bottle — — FDA listed —
Detox Drops Acne Toner 2 g/100mL 71499-0523-01 KENDO 1 bottle — — FDA listed —
FHF Day Breakthru 2 g/100g 72788-0142-11 Summer 1 bottle — — FDA listed —
Dr Throwers Oily Skin Facial Astringent 2 g/100g 72839-0611-02 Derma 57 g — — FDA listed —
Pore Refining Toner 2 g/100g 72957-0013-01 Private 195 g — — FDA listed —
Sunday Riley Peacekeeper Acne Treatment Serum 20 mg/mL 73001-0505-01 Sunday 1 pouch — — FDA listed —
Naturium Salicylic Acid Serum 2% 20 mg/mL 76354-0122-01 e.l.f. 1 bottle — — FDA listed —
e.l.f. PLZ Clarify Facial Oil 20 mg/mL 76354-0419-01 e.l.f. 1 bottle — — FDA listed —
The Inkey List 360 Acne Clearing Serum 20 mg/mL 81136-0028-01 Brand 1 bottle — — FDA listed —
Mara Clear Skin Mineral Milk Acne Treatment 20 mg/mL 81461-0002-00 Mara 30 ml — — FDA listed —
Dermeleve Scalp Psoriasis Treatment 2 g/100mL 81507-0006-01 Advanced 1 bottle — — FDA listed —
Peach and Lily Peaches Slices Acne Exfoliating toner 20 mg/mL 81515-0501-01 Peach 120 ml — — FDA listed —
Skinlycious Glow Exfoliant 2 g/100mL 81574-0001-01 Skinlycious 28 ml — — FDA listed —
CeraVe Developed with Dermatologists BHA Exfoliating Toner Acne Treatment 20 mg/mL 82046-0291-01 L'Oreal 237 ml — — FDA listed —
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 82046-0955-01 LOreal 1 bottle — — FDA listed —
Clarifying Toner 2 g/100mL 83286-0012-01 Drmtlgy, 189 ml — — FDA listed —
Bubble Super Clear Blemish Prevention Serum 20 mg/mL 83509-0001-01 BUBBLE 1 bottle — — FDA listed —
Doing The Work Salicylic Acid Acne Treatment 20 mg/mL 84234-0001-00 Personal 1 bottle — — FDA listed —
Personal Day Doing the Work Daily Exfoliating Treatment 20 mg/mL 84234-0002-00 Personal 1 bottle — — FDA listed —
Perricone MD Acne Relief Gentle Exfoliating Toner Salicylic Acid Acne Treatment 2 g/100mL 84448-0602-18 THG 1 bottle — — FDA listed —
AHA BHA Blemish Control and Exfoliating Serum 2 g/100mL 85439-0101-01 Banuskin, 30 ml — — FDA listed —
PHOFAY Salicylic Acid Acne Treatment Essence 20 mg/mL 87080-0001-00 Hangzhou 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

🏛️
2024
On the market since
Nov 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.

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

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 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 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 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 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • 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 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 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 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.
  • UNII 4YK5Z54AT2
    Denatonium benzoate is a bitter-tasting chemical compound added to medicines to discourage accidental ingestion, especially by children. It serves as a bittering agent with no therapeutic effect on the body.
  • UNII HOC5567T41
    A plant-derived compound from licorice root used as a preservative and antioxidant in medicines. It helps protect the product from degradation and extends shelf life.
  • 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 412ZHA4T4Y
    A plant-derived oil extracted from meadowfoam seeds. It acts as an emollient and skin-conditioning agent, helping soften and smooth the product texture while improving how it spreads on skin.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • 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 461N1O614Y
    A synthetic oily liquid used as an emollient and solvent in medications. It helps dissolve active ingredients and improves how the medicine spreads or absorbs through the skin.
  • 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 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.

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

The official label also statesCaprylic/CapricTriglyceride,Heianthus Annuus (Sunflower) Seed Oil Alcohol,Glycine Soja (Soybean)Oil,Octyldodecanol, 1,2-Hexanediol,Tocopherol,Melaleuca Altermifolia(Tea Tree)Leaf 0i,Bisabolol,Aloe Barbadensis Leaf Extract,Simmondsia Chinensis (Jojoba)Seed Oil,Limnanthes Alba(Meadowfoam)Seed Oil,Melia Azadirachta Leaf Extract,Melia Azadirachta Flower Extract,Corallina Officinalis Extract,Coccinia Indica Fuit Extact,Gabridn,Solanum Melongena (Eggplant)Fruit Extract,Aloe Barbadensis Fower Etract,Ocimum Sanctum Leaf Extract,Ocimum Baslicum(Basil) Flower/Leaf Extract,Curcuma Longa (Turmeric) Root Extract,Daucus Carota Sativa(Carrot) Root Extract,Beta-Carotene,Denatonium Benzoate,Limonene,Linalool May Contain:Yellow 11(Cl 47000)

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

LabelerZhejiang Ayan Biotech Co., Ltd.
FDA applicationM006 (OTC MONOGRAPH DRUG)
Labeler code70412
First marketedNov 2024
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from Zhejiang Ayan Biotech Co., Ltd. labeler code 70412

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 👥 Use in Specific Populations 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📋 Description 📄 Do Not Use 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 🔬 Clinical Studies 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

HOW TO USE: Massage 3-5 drops onto clean faceat night,avoiding the eye area.Theformula's green color will absorb fastwith a non-greasy feel.

⏱️ Dosage and Administration 87 words ▾

Directions ·Cleanse the skin thoroughy before applying medication.Cover the entire affected area wiha thin layer one to three times daily.Because excessivedrying of the skin may occu,start with one applicationdaly,then gradualy increase to two or three times dalyif neededor as directed by a doctor If bothersome dryness or peeling occurs,reduce application to once a day or every other day.Sensitivity Test for a New User.Apply product sparingly to one or twosmall affected areas during the first 3 days If no discomfort occurs,follow the directions stated elsewhere on this label.

⚠️ Warnings 5 words ▾

Warnings ·For external use only

👥 Use in Specific Populations 3 words ▾

SKIN TYPES: dry,combination,oily,sensitive,acne-prone

🧪 Active Ingredient 5 words ▾

Active Ingredients Salgylic Arid 2%

🧪 Inactive Ingredients 58 words ▾

Inactive Ingredients Caprylic/CapricTriglyceride,Heianthus Annuus (Sunflower) Seed Oil Alcohol,Glycine Soja (Soybean)Oil,Octyldodecanol, 1,2-Hexanediol,Tocopherol,Melaleuca Altermifolia(Tea Tree)Leaf 0i,Bisabolol,Aloe Barbadensis Leaf Extract,Simmondsia Chinensis (Jojoba)Seed Oil,Limnanthes Alba(Meadowfoam)Seed Oil,Melia Azadirachta Leaf Extract,Melia Azadirachta Flower Extract,Corallina Officinalis Extract,Coccinia Indica Fuit Extact,Gabridn,Solanum Melongena (Eggplant)Fruit Extract,Aloe Barbadensis Fower Etract,Ocimum Sanctum Leaf Extract,Ocimum Baslicum(Basil) Flower/Leaf Extract,Curcuma Longa (Turmeric) Root Extract,Daucus Carota Sativa(Carrot) Root Extract,Beta-Carotene,Denatonium Benzoate,Limonene,Linalool May Contain:Yellow 11(Cl 47000)

🎯 Purpose 13 words ▾

Purpose Acne Treatment

Use ·For the treatment of acne ·Helps prevent newacne blemishes

📋 Description 35 words ▾

WHAT IT DOES: Give stressed skin a moment of zen with this calming,non- comedogenic facial oil.Made with 2%BHA,a.k.a. salicylic acid,this formula helps treat and prevent new blackheads while clarifying clogged pores for a brighter-looking,even-toned complexion.

📄 Do Not Use 11 words ▾

Do not use ·Do not use on damaged or broken skin.

📄 When Using This Product 34 words ▾

When using this product skin iritation and dyness is more likely to occur if you use another topical acne medication at the same time.f iritation occurs,only use one topical acne medication at a time.

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Other Information 13 words ▾

Other Information ·Protect the product in thiscontainer from excessive heat and direct sun.

📄 Questions or Comments 2 words ▾

Questions? Questions?1-888-315-9814

🔬 Clinical Studies 4 words ▾

BEFORE &E.L.F.TER: BEFORE &E.L.F.TER:

📄 Package Label / Principal Display Panel 24 words ▾

PRINCIPAL DISPLAY PANEL PLZ CLARIFY FACIAL OIL CLARIFY+CALM 2%salicylic acid acne treatment+aloe extract e.l.f S KI N NET 1FL 0Z (30mL) principal display panel

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
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 Zhejiang Ayan Biotech Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Zhejiang Ayan Biotech Co., Ltd. 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.
← 70412-0338-10 · Zhejiang 70412-0411-06 · Zhejiang →
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.