Home › NDC Lookup › Ingredients › Avobenzone Octisalate Octocrylene › 70581-0020-03
Rener lift multi action ultra SPF 30 AVOBENZONE, OCTISALATE, OCTOCRYLENE 30 mg/mL; 50 mg/mL; 70 mg/mL Cream — NDC 70581-0020-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Rener lift multi action ultra SPF 30 AVOBENZONE, OCTISALATE, OCTOCRYLENE 30 mg/mL; 50 mg/mL; 70 mg/mL Cream — NDC 70581-020-03 (Billing 70581-0020-03)

by BPS 60 · 1 JAR in 1 CARTON / 75 mL in 1 JAR

This is a package of Rener lift multi action ultra SPF 30 AVOBENZONE, OCTISALATE, OCTOCRYLENE 30 mg/mL; 50 mg/mL; 70 mg/mL Cream from BPS 60, marketed since Mar 2022 and currently FDA-listed.

NDC 70581-0020-03
🏷️ FDA NDC (as labeled) 70581-020-03 billing pads the product segment with a zero
This package
Contains75 mL in 1 jar Pack sizes5 compare ↓
Product page 70581-0020-00 Also comes in: 5 mL 70581-020-00 30 mL 70581-020-01 50 mL 70581-020-02 15 ml 70581-020-04
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 70581-020-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
70581 labeler · 020 product · 03 package
Package marketed since
Mar 10, 2022
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
3614272727274, 3614272727281, 3614272727267
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 70581-020-03
Product NDC 70581-020
11-digit billing NDC 70581002003
UNII G63QQF2NOX, 4X49Y0596W, 5A68WGF6WM
UPC 3614272727274, 3614272727281, 3614272727267
Application # M020
SPL Set ID dad1db12-0e36-011e-e053-2995a90a54a1
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-03-10
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTISALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 70581-020-03 — 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 → 70581-0020-03. 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.

Clinical

🧪 What is this product?

This is a topical cream sunscreen marketed as an over-the-counter monograph product. It contains three active ingredients that function as ultraviolet (UV) filters: avobenzone, octisalate, and octocrylene. These ingredients are typically used together in sunscreen formulations to absorb and scatter UV radiation from the sun. The product is labeled with an SPF 30, indicating the sun protection factor level at which it is formulated.

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 gPer 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 30 mL 50 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
70581-0020-00 70581-020-00 Main listing 1 TUBE in 1 CARTON / 5 mL in 1 TUBE 2022-03-10 — Active
70581-0020-01 70581-020-01 1 JAR in 1 CARTON / 30 mL in 1 JAR 2022-03-10 — Active
70581-0020-02 70581-020-02 1 JAR in 1 CARTON / 50 mL in 1 JAR 2022-03-10 — Active
70581-0020-03 You're viewing this 1 JAR in 1 CARTON / 75 mL in 1 JAR 2022-03-10 — Active
70581-0020-04 70581-020-04 15 mL in 1 JAR 2022-03-10 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 jar in 1 carton / 75 ml in 1 jar.
What NDC number is used to bill for this package of Rener lift multi action ultra SPF 30 AVOBENZONE, OCTISALATE, OCTOCRYLENE 30 mg/mL; 50 mg/mL; 70 mg/mL Cream?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Seven Thirty Daily Habit Broad Spectrum SPF 30 30 mg/mL; 50 mg/mL; 70 mg/mL 85217-0582-00 SAN 74 ml — — FDA listed —
Jil Goorman Skincare Sun Guard SPF 30 30 mg/mL; 50 mg/mL; 70 mg/mL 85217-0581-00 SAN 74 ml — — FDA listed —
Rener lift multi action ultra SPF 30 30 mg/mL; 50 mg/mL; 70 mg/mLthis 70581-0020-03 BPS 1 jar — — FDA listed —
Atlanta Acne Specialist Everyday Sunscreen SPF 30 30 mg/mL; 50 mg/mL; 70 mg/mL 85217-0583-00 SAN 74 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

🏛️
2022
On the market since
Mar 2022
📍
2026
Currently FDA-listed
4 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 AU6XZE9IY9
    A natural wax derived from acacia decurrens flowers. It functions as a coating agent, lubricant, and polish to give tablets and capsules a smooth, protective finish and improve handling during manufacturing.
  • UNII K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • 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 KBC00G95HI
    A synthetic polymer used primarily as a thickener and stabilizer in topical formulations. It helps create the desired texture and consistency while keeping ingredients evenly distributed throughout the product.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII OEB4R3WW9C
    A silicone-based emulsifier and anti-foaming agent derived from polyethylene glycol. It helps prevent foam formation during manufacturing and aids in blending oil and water components in liquid formulations.
  • UNII 5F7PJF6AA4
    A fatty acid derivative that combines salicylic acid with a plant-derived oil component. It acts as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 9DBA0SBB0L
    A synthetic red dye derived from coal tar used as a colorant in medicines and cosmetics. It gives tablets, capsules, and liquids their red or pink appearance for identification and visual appeal.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 45ASM2L11M
    A synthetic ingredient derived from glutamic acid and stearic acid. It acts as an emulsifier and surfactant, helping oils and water mix smoothly in the medication formulation.
  • 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 L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • 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 12133JR80S
    Guanosine is a natural nucleoside compound derived from nucleic acids. In medicines, it may serve as a buffer or pH regulator to help stabilize the formulation and maintain proper acidity levels.
  • UNII 42DG15CHXV
    A natural plant wax derived from sunflower seeds. It serves as a lubricant and glidant to help powders flow smoothly during manufacturing and tablet formation.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII S4V5BS6GCX
    A synthetic oily liquid used as an emollient and solvent in topical medications. It helps dissolve active ingredients and creates a smooth, spreadable texture on the skin.
  • UNII QQC1AK06RK
    A botanical extract from alpine edelweiss flowers used as a natural fragrance, flavor component, or skin-conditioning agent in topical or oral formulations. It may also serve antioxidant or soothing purposes in finished products.
  • UNII GFD7C86Q1W
    A natural oil extracted from citrus peels, (+)-limonene is used as a flavoring agent and solvent in medicines. It helps dissolve active ingredients and provides a lemon or orange taste.
  • 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 762O8IWA10
    PEG-8 laurate is a synthetic compound made by combining polyethylene glycol with lauric acid. It acts as an emulsifier and solubilizer in medicines, helping to blend water and oil-based ingredients together and improve how well some drugs dissolve.
  • 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 4A0NCJ6RD6
    Polyglycerin-3 is a synthetic ingredient made by linking multiple glycerin molecules together. It acts as an emulsifier and humectant, helping oils and water mix smoothly and keeping the product from drying out.
  • UNII Z35I17EQOP
    A waxy substance made from glycerin and stearic acid that helps stabilize and thicken cosmetic and pharmaceutical formulations. It works as an emulsifier to blend oil and water-based ingredients together.
  • 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 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII 7J95K7ID2S
    A plant extract from the roots of Chinese skullcap, used as a natural coloring agent and to add mild flavor to medicines. It may also help preserve the product's stability.
  • 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 554127163Y
    Sodium dodecylbenzenesulfonate is a synthetic detergent and surfactant used in medicines to help dissolve or suspend active ingredients and improve how the product flows and mixes during manufacturing.
  • 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 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 9NH1UDD2RR
    A synthetic silicone polymer that forms a smooth, water-resistant film. Used in topical formulations as a skin protectant coating and to improve product texture and spreadability on the skin.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also stateswater, glycerin, dimethicone, isononyl isononanoate, propanediol, vinyl dimethicone/methicone silsesquioxane crosspolymer, alcohol denat., bis-PEG-18 methyl ether dimethyl silane, polyglyceryl-6 distearate, jojoba esters, tocopherol, limnanthes alba (meadowfoam) seed oil, acacia decurrens flower wax, guanosine, sodium hyaluronate, hydrolyzed linseed extract, sodium hydroxide, sodium dodecylbenzenesulfonate, sodium benzoate, RED 33, phenoxyethanol, adenosine, PEG-8 laurate, helianthus annuus (sunflower) seed wax, polyglyceryl-3 beeswax, polyglycerin-3, ammonium acryloyldimethyltaurate/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolymer, dimethiconol, limonene, xanthan gum, benzyl alcohol, leontopodium alpinum flower/leaf extract, capryloyl salicylic acid, caprylyl glycol, geraniol, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, citric acid, potassium sorbate, scutellaria baicalensis root extract, styrene/acrylates copolymer, fragrance

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

LabelerBPS 60
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code70581
First marketedMar 2022
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from BPS 60 labeler code 70581

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

Uses helps prevent sunburn if used as directed with other sun protection measures (see ), decreases the risk of skin cancer and early skin aging caused by the sun Directions

⏱️ Dosage and Administration 98 words ▾

Directions: For sunscreen use: apply generously and evenly 15 minutes before sun exposure reapply at least every 2 hours use a water resistant sunscreen if swimming or sweating Spending time in the sun increases your risk of skin cancer and early sking aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures. limit time in the sun, especially from 10 a.m. - 2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses.

Children under 6 months of age: Ask a doctor.

⚠️ Warnings 66 words ▾

Warnings: For external use only. Do not use near fire, flame or heat. Flammable until dry. Do not use on damaged or broekn skin When using this product keep out of eyes. Rinse with water to remove. Stop use and and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 10 words ▾

Active ingredients: Avobenzone 3% Octisalate 5% Octocrylene 7% Purpose: Sunscreen.

🧪 Inactive Ingredients 100 words ▾

Inactive ingredients water, glycerin, dimethicone, isononyl isononanoate, propanediol, vinyl dimethicone/methicone silsesquioxane crosspolymer, alcohol denat., bis-PEG-18 methyl ether dimethyl silane, polyglyceryl-6 distearate, jojoba esters, tocopherol, limnanthes alba (meadowfoam) seed oil, acacia decurrens flower wax, guanosine, sodium hyaluronate, hydrolyzed linseed extract, sodium hydroxide, sodium dodecylbenzenesulfonate, sodium benzoate, RED 33, phenoxyethanol, adenosine, PEG-8 laurate, helianthus annuus (sunflower) seed wax, polyglyceryl-3 beeswax, polyglycerin-3, ammonium acryloyldimethyltaurate/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolymer, dimethiconol, limonene, xanthan gum, benzyl alcohol, leontopodium alpinum flower/leaf extract, capryloyl salicylic acid, caprylyl glycol, geraniol, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, citric acid, potassium sorbate, scutellaria baicalensis root extract, styrene/acrylates copolymer, fragrance

🎯 Purpose 2 words ▾

Purpose: Sunscreen.

📄 Do Not Use 8 words ▾

Do not use on damaged or broekn skin

📄 When Using This Product 13 words ▾

When using this product keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 10 words ▾

Stop use and and ask a doctor if rash occurs.

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Questions or Comments 14 words ▾

Questions or comments? Monday - Friday (9 a.m. - 5 p.m. EST) 1-800-LANCOME (1-800-526-2663)

📄 Package Label / Principal Display Panel 36 words ▾

Package Labeling:70581-020-04 Label 15ml

Package Labeling:70581-020-01 Label 30ml Label2 30ml Label3 30ml

Package Labeling:70581-020-00 Label 5ml Label2 5ml Label3 5ml

Package Labeling:70581-020-02 Label 50ml Label2 50ml Label3 50ml

Package Labeling:70581-020-03 Label 75ml Label2 75ml Label3 75ml

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

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 AVOBENZONE, OCTISALATE, OCTOCRYLENE — the ingredient across all brands.

Top reported reactions

Rash3
Skin Cancer3
Application Site Burn2
Hypersensitivity2
Product Expiration Date Issue2
Product Lot Number Issue2
Acne1

Reporter sex

0 reports

Serious outcomes

Hospitalization1
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 2 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 BPS 60. 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 4 other package presentations of this same product, including 1 tube (70581-0020-00), 1 jar (70581-0020-01), 1 jar (70581-0020-02). 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?
BPS 60 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.
← 70581-0019-00 · BPS 70594-0023-01 · Xellia →
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.