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Mary Kay TimeWise Miracle Set 3D The Go Set (Combo to Oily Skin) Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone Kit — NDC 51531-9020-0 (Billing 51531-9020-00)

by Mary Kay Inc. · 1 KIT in 1 CARTON * 9 g in 1 TUBE * 3 g in 1 TUBE * 9 g in 1 TUBE * 14 g in 1 TUBE

This is a package of Mary Kay TimeWise Miracle Set 3D The Go Set (Combo to Oily Skin) Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone Kit from Mary Kay Inc., no longer marketed (first marketed May 2018), no longer in the FDA NDC Directory, this package's marketing ended Jul 2026. It is this product's only package size.

NDC 51531-9020-00
🏷️ FDA NDC (as labeled) 51531-9020-0 billing pads the package segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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 51531-9020-0 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
51531 labeler · 9020 product · 0 package
Package marketed since
May 16, 2018
Package marketing ended
Jul 31, 2026
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 5153190200 5
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jul 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 51531-9020-0
Product NDC 51531-9020
11-digit billing NDC 51531902000
Application # M020
SPL Set ID fb20d1e6-0de2-4a81-9432-1f8eeefe6eff
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jul 2026)
Marketing start 2018-05-16
Marketing end 2026-07-31
Dosage form KIT
Why two NDCs? The FDA registers this code as 51531-9020-0 — a 5-4-1 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 package segment → 51531-9020-00. 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.

Clinical

🧪 What is this product?

This is a skincare kit containing sunscreen products marketed under FDA's over-the-counter monograph rules. The active ingredients (avobenzone, homosalate, octisalate, octocrylene, and oxybenzone) are ultraviolet (UV) filters typically used in sunscreen formulations to help protect skin from sun exposure. The kit is designed for combination to oily skin types and includes multiple products meant to be used together as part of a daily skincare routine.

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 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.
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
51531-9020-00 You're viewing this Main listing 1 KIT in 1 CARTON * 9 g in 1 TUBE * 3 g in 1 TUBE * 9 g in 1 TUBE * 14 g in 1 TUBE 2018-05-16 Jul 31, 2026 Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Mary Kay TimeWise Repair Volu-Firm Set 51531-8434-00 Mary 1 kit — — FDA listed —
Obagi Skintrinsiq Antioxidant Protocol 62032-0907-07 Obagi 1 kit — — Discontinued —
Mary Kay TimeWise Repair Volu-Firm Sampler Set 51531-1606-00 Mary 1 kit — — FDA listed —
Mary Kay TimeWise Miracle Set 3D The Go Set (Combo to Oily Skin)this 51531-9020-00 Mary 1 kit — — Discontinued —
Mary Kay TimeWise Repair Volu-Firm The Go Set 51531-1614-00 Mary 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.

Availability & generic status

🏛️
2018
On the market since
May 2018
📍
2026
Currently FDA-listed
8 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
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.

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

LabelerMary Kay Inc.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code51531
First marketedMay 2018
Product typeHuman Otc Drug
Portfolio21 products on file

More NDCs from Mary Kay Inc. labeler code 51531

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 📦 Storage and Handling 🧪 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 Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

⏱️ Dosage and Administration 90 words ▾

Directions apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m. - 2 p.m. wear long-sleeve shirts, pants, hats, and sunglasses children under 6 months: Ask a doctor

⚠️ Warnings 56 words ▾

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

📦 Storage and Handling 18 words ▾

Other information protect this product from excessive heat and direct sun store above 32° F / 0° C

🧪 Active Ingredient 14 words ▾

Active ingredients Avobenzone 3% Homosalate 9% Octisalate 4.5% Octocrylene 3% Oxybenzone 4.5% Purpose Sunscreen

🧪 Inactive Ingredients ~1 min read ▾

Ingredients WATER, TEA-LAURYL SULFATE, ACRYLATES COPOLYMER, PROPANEDIOL, COCAMIDOPROPYL BETAINE, TRIETHANOLAMINE, PPG-2 HYDROXYETHYL COCO/ISOSTEARAMIDE, COPERNICIA CERIFERA (CARNAUBA) WAX, NIACINAMIDE, GLYCERIN, OLIGOPEPTIDE-1, RESVERATROL, CELLULOSE, LACTOSE, HYDROXYPROPYL METHYLCELLULOSE, HYDROXYPROPYL CYCLODEXTRIN, CITRIC ACID, SODIUM CHLORIDE, METHYLDIHYDROJASMONATE, ETHYLENE BRASSYLATE, ETHYL LINALOOL, TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES, ISOBUTYL METHYL TETRAHYDROPYRANOL, METHYLENEDIOXYPHENYL METHYLPROPANAL, PHENYLISOHEXANOL, TRIMETHYLBENZENEPROPANOL, METHYL BENZODIOXEPINONE, DISODIUM EDTA, IODOPROPYNYL BUTYLCARBAMATE, MAGNESIUM CHLORIDE, MAGNESIUM NITRATE, METHYLISOTHIAZOLINONE, METHYLCHLOROISOTHIAZOLINONE, TALC, RED 30, ULTRAMARINES.

Inactive ingredients water/eau, glycerin, dicaprylyl carbonate, dimethicone, ammonium acryloyldimethyltaurate/VP copolymer, cetearyl alcohol, ceteareth-25, niacinamide, opuntia ficus-indica fruit extract, saccharomyces cerevisiae extract, tocopheryl acetate, oligopeptide-1, resveratrol, sucrose palmitate, bisabolol, silica, disodium ethylene dicocamide PEG-15 disulfate, hydroxypropyl cyclodextrin, glyceryl linoleate, ethoxydiglycol, methyldihydrojasmonate, ethylene brassylate, tetramethyl acetyloctahydronaphthalenes, ethyl linalool, isobutyl methyl tetrahydropyranol, methylenedioxyphenyl methylpropanal, phenylisohexanol, trimethylbenzenepropanol, methyl benzodioxepinone, triethanolamine, sodium benzoate, disodium EDTA, caprylhydroxamic acid, phenoxyethanol, ethylhexylglycerin, propanediol, caprylyl glycol, iodopropynyl butylcarbamate.

INGREDIENTS: WATER, GLYCERIN, ISOHEXADECANE, BUTYLENE GLYCOL, ALUMINUM STARCH OCTENYLSUCCINATE, ISOCETYL STEARATE, CETYL ALCOHOL, CETYL ESTERS, CAPRYLYL METHICONE, NIACINAMIDE, CETEARYL ALCOHOL, GLYCERYL STEARATE, OLIGOPEPTIDE-1, RESVERATROL, PRUNUS MUME LEAF EXTRACT, ARACHIDYL GLUCOSIDE, ACRYLAMIDE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER, CAPRYLIC/CAPRIC TRIGLYCERIDE, STEARIC ACID, TOCOPHERYL ACETATE, PANTHENOL, SUCROSE PALMITATE, PEG-100 STEARATE, ARACHIDYL ALCOHOL, DIMETHICONE, CETEARETH-20, BEHENYL ALCOHOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, XANTHAN GUM, POLYSORBATE 80, HYDROXYPROPYL CYCLODEXTRIN, GLYCERYL LINOLEATE, ETHOXYDIGLYCOL, METHYLDIHYDROJASMONATE, ETHYLENE BRASSYLATE, TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES, ETHYL LINALOOL, ISOBUTYL METHYL TETRAHYDROPYRANOL, METHYLENEDIOXYPHENYL METHYLPROPANAL, PHENYLISOHEXANOL, TRIMETHYLBENZENEPROPANOL, METHYL BENZODIOXEPINONE, TRIETHANOLAMINE, DISODIUM EDTA, PHENOXYETHANOL, 1,2-HEXANEDIOL, HYDROXYACETOPHENONE, CAPRYLYL GLYCOL, IODOPROPYNYL BUTYLCARBAMATE, TITANIUM DIOXIDE.

INGREDIENTS: WATER/EAU, CETYL ALCOHOL, GLYCERIN, C12-15 ALKYL BENZOATE, STEARIC ACID, GLYCERYL STEARATE, PEG-100 STEARATE, 1,2-HEXANEDIOL, NIACINAMIDE, ALGAE EXTRACT, OLIGOPEPTIDE-1, PANTHENOL, RESVERATROL, TOCOPHERYL ACETATE, DIPOTASSIUM GLYCYRRHIZATE, XANTHAN GUM, HEXYLENE GLYCOL, DIMETHICONE, POLYMETHYL METHACRYLATE, TRICAPRYLIN, ETHYLHEXYL PALMITATE, SILICA, HYDROXYPROPYL CYCLODEXTRIN, TRIETHANOLAMINE, DISODIUM EDTA, BENZYL ALCOHOL, CAPRYLYL GLYCOL, IODOPROPYNYL BUTYLCARBAMATE, MICA, TITANIUM DIOXIDE.

🎯 Purpose 2 words ▾

Purpose Sunscreen

📄 Do Not Use 8 words ▾

Do not use on damaged or broken 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 9 words ▾

Stop use and ask a doctor if rash occurs

📄 Keep Out of Reach of Children 21 words ▾

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

📄 Questions or Comments 6 words ▾

Questions or comments? Call toll-free 1-800-627-9529

📄 Package Label / Principal Display Panel 81 words ▾

Principal Display Panel - The Go Set Combo/Oily carton Mary Kay TimeWise Miracle Set 3D The Go Set contains: 1 Age Minimize 3D 4-in-1 Cleanser .5 OZ. NET WT. / 14 g 1 Age Minimize 3D Day Cream SPF 30 Broad-Spectrum Sunscreen .3 OZ. NET WT. / 9 g 1 Age Minimize 3D Night Cream .3 OZ. NET WT. / 9 g 1 Age Minimize Eye Cream .1 OZ. NET WT. / 3 g image of The Go Set C/O carton

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, Homosalate, Octisalate, Octocrylene, and Oxybenzone — the ingredient across all brands.

Top reported reactions

Skin Cancer32
Basal Cell Carcinoma14
Neoplasm Malignant13
Malignant Melanoma12
Rash11
Burns Third Degree9
Recalled Product Administered7

Age at onset

Infant1
Child1
Adolescent1
Adult28
Elderly8

Reporter sex

155 reports
Male · 39%
Female · 61%

Serious outcomes

Hospitalization6
Disabling5
Death5
Life-threatening2
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 5 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 Kit / multi-component package No longer marketed (per FDA listing data)

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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
Mary Kay 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.
← 51531-8977-00 · Mary 51531-9071-00 · Mary →
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.