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Brush and Go Oily Problematic Skin Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g Powder, 5 g — NDC 78863-1012-02 package photo

Brush and Go Oily Problematic Skin Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g Powder, 5 g

by Noon Aesthetics M.R. Ltd · 5 g in 1 BOTTLE, WITH APPLICATOR (78863-1012-2)
NDC 78863-1012-02
🏷️ FDA NDC (as labeled) 78863-1012-2 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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) 78863-1012-2
Product NDC 78863-1012
11-digit billing NDC 78863101202
UNII 4Y5P7MUD51, 95OOS7VE0Y, 5A68WGF6WM, 4X49Y0596W, 15FIX9V2JP, G63QQF2NOX
Application # M020
SPL Set ID b4295453-f193-4bed-be5b-efcd91772107
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-05-01
Route TOPICAL
Dosage form POWDER
Substance TITANIUM DIOXIDE; OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE; OXYBENZONE
Why two NDCs? The FDA registers this code as 78863-1012-2 — 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 → 78863-1012-02. 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.

🏭 Manufacturer & labeler

LabelerNoon Aesthetics M.R. Ltd
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code78863
First marketedMay 2020
Product typeHuman Otc Drug
Portfolio21 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 is this product?

Brush and Go Oily Problematic Skin is an over-the-counter powder product applied to the skin that contains multiple sun-protective ingredients. Avobenzone, octinoxate, octisalate, octocrylene, and oxybenzone are chemical UV filters typically used to absorb ultraviolet radiation. Titanium dioxide is a mineral sun filter that works by reflecting UV rays. Together, these ingredients function as a sunscreen product intended for topical use on oily or acne-prone skin types.

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.

💊 What it looks like

Color Brown
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 1P9D0Z171K
    BHT is a synthetic antioxidant that prevents fats and oils in medicines from breaking down and becoming rancid. It helps keep the product stable and effective during storage.
  • 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 72T9EZC2VX
    Eucalyptus gum is a natural plant resin extracted from eucalyptus trees. It acts as a binder and thickening agent to hold tablet or capsule ingredients together and improve texture in liquid formulations.
  • UNII 1K09F3G675
    Ferric oxide red is an inorganic iron compound used as a colorant in medicines. It gives tablets, capsules, or other dosage forms a red or reddish tint for identification and appearance.
  • UNII EX438O2MRT
    Ferric oxide yellow is a naturally occurring iron compound used as a colorant in medications. It gives tablets, capsules, and other forms a yellow or golden hue for identification and appearance.
  • UNII XM0M87F357
    A dark iron oxide compound that gives medicines their black or dark color. It's used as a colorant in tablets and capsules to help identify the product and make it visually distinctive.
  • UNII WB5K9Y35Y9
    A synthetic crosslinked polymer made by combining hexamethylene diisocyanate with trimethylol hexyllactone. It's used as a film-former and binder to help create protective coatings on tablets or capsules and improve product stability.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • UNII H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • UNII 4PW41QCO2M
    Indian frankincense is a natural resin extracted from trees native to India. It is used in medicines as a binder and thickening agent to help hold ingredients together and improve texture.
  • UNII EG97988M5Q
    A synthetic plastic polymer that forms a three-dimensional network. It's used as a coating on tablets and capsules to control how fast the medicine releases into the body, or as a binder to hold pill ingredients together.
  • UNII V8A1AW0880
    Mica is a naturally occurring mineral that's ground into fine powder. It's used in medicines as a colorant and anti-caking agent to improve appearance and prevent clumping in tablets or powders.
  • UNII Q46328TRNK
    A short-chain protein fragment made of 10 amino acids linked together. Used in formulations as a skin-conditioning agent or penetration enhancer to help active ingredients absorb into skin or improve product texture.
  • 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 59Z907ZB69
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles, helping powders and tablets flow smoothly during manufacturing and use.
  • 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 ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII 3M4G523W1G
    Silver is a metallic element used in some medications as an antimicrobial agent in topical formulations. It helps prevent bacterial growth on wound dressings and certain skin preparations.
  • 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 18L31PSR28
    Trimyristin is a fatty substance derived from plant or animal sources. It acts as a lubricant and binder in tablets and capsules, helping the medicine hold together and move smoothly through manufacturing equipment.
  • 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.

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

The official label also statesMica, Methyl Methacrylate Crosspolymer, Aloe Barbadensis Leaf Juice, BHT, Silica, Maris Limus (Dead Sea Mineral Mud), Polymethylsilsesquioxane, HDI/Trimethylol Hexyllactone Crosspolymer, Oligopeptide-10,Silver, Curcuma Longa (Turmeric) Root extract, Boswellia Serrata Extract, Honey Extract, Trimyristin, Hydrogenated Lecithin, Phenoxyethanol, Caprylyl glycol, Potassium Sorbate, Hexylene Glycol, Eucalyptus, Tea Tree Oil, CI 77492,Hydrogenated Lecithin, CI 77491, ci 77499.

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 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.
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
Brush and Go All Skin types 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g 78863-1010-01 Noon 5 g — — FDA listed —
Brush and Go All Skin types Matte Finish Tone 1 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g 78863-1011-01 Noon 2 bottles — — FDA listed —
Brush and Go Oily Problematic Skin 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5gthis 78863-1012-02 Noon 5 g — — FDA listed —
Brush and Go All Skin types Matte Finish Tone 2 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g 78863-1013-01 Noon 2 bottles — — FDA listed —
Brush and Go Oily Problematic Skin Matte Finish Tone 1 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g 78863-1016-02 Noon 2 bottles — — FDA listed —
Brush and Go Oily Problematic Skin Matte Finish Tone 2 1.25 g/5g; .236 g/5g; .225 g/5g; .135 g/5g; .075 g/5g; .075 g/5g 78863-1017-02 Noon 2 bottles — — 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

🏛️
2020
On the market since
May 2020
📍
2026
Currently FDA-listed
6 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
78863-1012-02 You're viewing this 5 g in 1 BOTTLE, WITH APPLICATOR (78863-1012-2) 2020-05-01 Active

🧭 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 78863-1012-2, 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: 78863-1012-02, written without dashes as 78863101202. 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 78863-1012-02, the first segment (78863) is the labeler code FDA assigned to Noon Aesthetics M.R. Ltd; the middle segment (1012) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Noon Aesthetics M.R. Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Noon Aesthetics M.R. 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.

📄 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
🎯 Indications and Usage 4 words ▾

Use Help prevent sunburn

⏱️ Dosage and Administration 20 words ▾

Directions Apply generously 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor for sunscreen use

⚠️ Warnings 57 words ▾

Warnings For external use only Do not use on damage 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 11 words ▾

Other information Protect this product from excessive heat and direct sun.

🧪 Active Ingredient 18 words ▾

Active Ingredients Titanium Dioxide 25% Ethylhexyl Methoxycinnamate 4.7% Octocrylene 4.5% Ethylhexyl Salicylate 2.7% Butyl Methoxydibenzoylmethane 1.5% Benzophenone 1.5%

🧪 Inactive Ingredients 55 words ▾

Inactive Ingredients Mica, Methyl Methacrylate Crosspolymer, Aloe Barbadensis Leaf Juice, BHT, Silica, Maris Limus (Dead Sea Mineral Mud), Polymethylsilsesquioxane, HDI/Trimethylol Hexyllactone Crosspolymer, Oligopeptide-10,Silver, Curcuma Longa (Turmeric) Root extract , Boswellia Serrata Extract, Honey Extract, Trimyristin, Hydrogenated Lecithin, Phenoxyethanol, Caprylyl glycol, Potassium Sorbate, Hexylene Glycol, Eucalyptus, Tea Tree Oil, CI 77492,Hydrogenated Lecithin, CI 77491, ci 77499.

🎯 Purpose 2 words ▾

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 78863-1011-01 · Noon 78863-1013-01 · Noon →
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.