NDC 78863-3003-02 — BRUSH and GO SPF 50 ALL SKIN TYPES BROAD

🆔 Identity & classification

FDA NDC (as labeled) 78863-3003-2

Product NDC 78863-3003

11-digit billing NDC 78863300302

UNII 15FIX9V2JP, 4Y5P7MUD51, 5A68WGF6WM, 4X49Y0596W, G63QQF2NOX, 95OOS7VE0Y

Application # M020

SPL Set ID 0d9f132c-7630-4261-a0f8-fc7a4377731f

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2024-04-01

Route TOPICAL

Dosage form POWDER

Substance TITANIUM DIOXIDE; OCTINOXATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE; OXYBENZONE

Why two NDCs? The FDA registers this code as 78863-3003-2 — 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 → 78863-3003-02. 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 marketedApr 2024

Product typeHuman Otc Drug

Portfolio21 products on file

🔎 All NDCs from Noon Aesthetics M.R. Ltd

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 SPF 50 is a topical powder sunscreen sold over the counter under FDA's OTC monograph rules for sunscreen products. It contains six active ingredients that function as ultraviolet (UV) filters: titanium dioxide and avobenzone, octinoxate, octisalate, octocrylene, and oxybenzone. These mineral and chemical UV-blocking agents are commonly included in sunscreen formulations intended to help protect skin from sun exposure. The product is designed for all skin types and provides broad-spectrum coverage.

Patient education

📘 MedlinePlus patient leaflet ↗

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 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 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 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 70097M6I30
Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
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 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 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 JB2MV9I3LS
Stannous oxide is a tin-based compound used as a polishing agent in toothpaste formulations. It helps remove surface stains and create a smooth tooth surface during brushing.

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

The official label also statesMica, Methyl Methacrylate Crosspolymer, Magnesium Stearate, Silica, CI 77492, CI 77491, CI 77499, Silt (Dead Sea Mineral Mud), Aloe Barbadensis Leaf Juice, Tin Oxide, Hydrogenated Lecithin, Phenoxyethanol, BHT, Caprylyl Glycol

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 system	Per g	Per 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: 2 bottles

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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
BRUSH and GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM .75 g/5mL; .141 g/5mL; .135 g/5mL; .08 g/5mL; .045 g/5mL; .045 g/5mLthis 78863-3003-02	Noon	3 bottles	—	—	FDA listed	—
BRUSH and GO SPF 50 OILY/PROBLEMATIC SKIN BROAD SPECTRUM .75 g/5mL; .141 g/5mL; .135 g/5mL; .08 g/5mL; .045 g/5mL; .045 g/5mL 78863-3004-01	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

🏛️

2024

On the market since

Apr 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.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
78863-3003-01	2 BOTTLE, PLASTIC in 1 CARTON (78863-3003-1) / 5 mL in 1 BOTTLE, PLASTIC	2024-04-01	Active
78863-3003-02 You're viewing this	3 BOTTLE, PLASTIC in 1 CARTON (78863-3003-2) / 5 mL in 1 BOTTLE, PLASTIC	2024-04-01	Active

Pack size FAQ

What quantity is in NDC 78863-3003-02?

NDC 78863-3003-02 is listed by the FDA — 3 bottle, plastic in 1 carton / 5 ml in 1 bottle, plastic.

What NDC number is used to bill for this package of BRUSH and GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, and OXYBENZONE .75 g/5mL; .141 g/5mL; .135 g/5mL; .08 g/5mL; .045 g/5mL; .045 g/5mL Powder?

Bill NDC 78863-3003-02 — the 11-digit billing format is 78863300302. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product

What data is (and isn’t) available for this NDC — tap to expand

NDC identity (package / product / labeler codes)	✓ Available
Labeler	✓ Available
Product & package description	✓ Available
Marketing category & status	✓ Available
Active ingredient / dosage form / route	✓ Available
FDA label (SPL via DailyMed)	✓ Available
Package photos	✓ Available
Inactive ingredients (structured)	✓ Available
NADAC pharmacy acquisition price (CMS)	— Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data	— Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk	— Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD)	— Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.

“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?

An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.

Why is there no price listed?

The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.

Is the NDC printed on the package the same as the 11-digit billing NDC?

Yes, they identify this exact package in different formats. The FDA registers it as 78863-3003-2, 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: 78863-3003-02, written without dashes as 78863300302. 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 78863-3003-02, the first segment (78863) is the labeler code FDA assigned to Noon Aesthetics M.R. Ltd; the middle segment (3003) 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.

Does this product come in other package sizes?

Yes — the FDA directory lists 1 other package presentation of this same product, including 2 bottles (78863-3003-01). 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?

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 ▾

Uses Helps prevent sunburn.

⏱️ Dosage and Administration 91 words ▾

Directions Apply liberally 15 minutes before sun exposure and as needed. Use a water-resistant sunscreen if swimming or sweating. Reapply at least every 2 hours.

Children under 6 months: Ask a doctor. 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 value 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-sleeved shirts, pants, hats, and sunglasses.

⚠️ Warnings 58 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 or irritation develops and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 29 words ▾

Other Information Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

🧪 Active Ingredient 26 words ▾

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

🧪 Inactive Ingredients 32 words ▾

Inactive Ingredients Mica, Methyl Methacrylate Crosspolymer, Magnesium Stearate, Silica, CI 77492, CI 77491, CI 77499, Silt (Dead Sea Mineral Mud), Aloe Barbadensis Leaf Juice, Tin Oxide, Hydrogenated Lecithin, Phenoxyethanol, BHT, Caprylyl Glycol

🎯 Purpose 26 words ▾

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

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

🔗 Related NDC lookups

🧪 All Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, And Oxybenzone NDCsSame ingredient 🏭 All Noon labeler NDCsLabeler code 78863