Home › NDC Lookup › Ingredients › Homosalate, Octocrylene, Ethylhexyl Sali... › 72220-0002-02
MDP PEPTIDE 9 BIO SUN PRO Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane 9.5 g/100g; 5 g/100g; 2.7 g/100g; 4.5 g/100g Stick, 20 g — NDC 72220-0002-02 package photo

MDP PEPTIDE 9 BIO SUN PRO Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane 9.5 g/100g; 5 g/100g; 2.7 g/100g; 4.5 g/100g Stick, 20 g

by SKINIDEA CO., LTD · 1 CONTAINER in 1 CARTON (72220-002-02) / 20 g in 1 CONTAINER (72220-002-01)
NDC 72220-0002-02
🏷️ FDA NDC (as labeled) 72220-002-02 billing pads the product segment with a zero
This package
Contains20 g Pack sizes2 compare ↓
Also comes in: 20 g 72220-0002-04
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 72220-002-02
Product NDC 72220-002
11-digit billing NDC 72220000202
UNII V06SV4M95S, 5A68WGF6WM, G63QQF2NOX, 4X49Y0596W
Application # M020
SPL Set ID 26db53cd-dd82-8790-e063-6394a90a92b1
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-11-01
Route TOPICAL
Dosage form STICK
Substance HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 72220-002-02 — 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 → 72220-0002-02. 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

LabelerSKINIDEA CO., LTD
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code72220
First marketedNov 2024
Product typeHuman Otc Drug
Portfolio2 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?

MDP Peptide 9 Bio Sun Pro is an over-the-counter sunscreen stick containing four UV-filtering agents: homosalate, octisalate, octocrylene, and avobenzone. These ingredients are typically used together to absorb and scatter ultraviolet rays from the sun. This topical product is marketed under FDA's sunscreen monograph rules, which allow combinations of established UV filters to be sold without individual product approval. It is applied directly to the skin for sun protection.

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.

🧪 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 YCD50O0Z6L
    A synthetic oily liquid used as a solvent and conditioning agent in topical formulations. It helps dissolve other ingredients and improves how the product spreads and feels on skin.
  • UNII J8T3X564IH
    A clear oily liquid derived from sebacic acid, used as a plasticizer and solvent in pharmaceutical coatings and films to improve flexibility and help active ingredients dissolve properly.
  • 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.

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

The official label also statesInactive ingredients Dimethicone, Methyl Methacrylate Crosspolymer, Synthetic Wax, Diethylhexyl Carbonate, Diisopropyl Sebacate, Diphenylsiloxy Phenyl Trimethicone, Isopropyl Palmitate, Polymethyl Methacrylate, Caprylyl Trimethicone, Diisostearyl Malate, Phenethyl Benzoate, Acrylates Copolymer, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyloctyl Salicylate, Polyethylene, Dimethicone/Vinyl Dimethicone Crosspolymer, Curcuma Longa (Turmeric) Root Extract, Camellia Japonica Seed Oil, Melia Azadirachta Flower Extract, Melia Azadirachta Leaf Extract, Corallina Officinalis Extract, Melia Azadirachta Bark Extract, Moringa Oleifera Seed Oil, Ocimum Sanctum Leaf Extract, Hydrolyzed Hyaluronic Acid, Collagen Amino Acids, Haematococcus Pluvialis Extract, Collagen, Aloe Barbadensis Leaf Extract, Dioscorea Japonica Root Extract, Laminaria Japonica Extract, Sodium Hyaluronate, Ulmus Davidiana Root Extract, Viola Mandshurica Flower Extract, Heptasodium Hexacarboxymethyl Dipeptide-12, Anemarrhena Asphodeloides Root Extract, Hyaluronic Acid, Collagen Extract, Microcrystalline Wax, Polymethylsilsesquioxane, Ethylene/Propylene Copolymer, Silica Dimethyl Silylate, Dimethicone Crosspolymer, Water, Butylene Glycol, Ectoin, Ubiquinone, Hydrogenated Polyisobutene, Glycerin, 1,2-Hexanediol, Propanediol, Sorbitan Laurate, Hydroxyethylcellulose, Acetyl Dipeptide-1 Cetyl Ester, Hydroxypropyltrimonium Hyaluronate, Acetyl Hexapeptide-8, Ascorbic Acid Polypeptide, Dextran, Hexapeptide-9, Sodium Acetylated Hyaluronate, Tripeptide-1, Tocopherol, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, Acetyl Octapeptide-3, Acetyl Tetrapeptide-2, Acetyl Tetrapeptide-3, Acetyl Tetrapeptide-5, Acetyl Tetrapeptide-9, Carnosine, Copper Tripeptide-1, Nonapeptide-1, Palmitoyl Pentapeptide-4, Palmitoyl Tripeptide-1, Palmitoyl Tripeptide-5, 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.

💲 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.
Try another pack size: 20 g
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
Mdp Peptide 9 Bio Sun Pro 9.5 g/100g; 5 g/100g; 2.7 g/100g; 4.5 g/100gthis 72220-0002-02 SKINIDEA 20 g — — 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
72220-0002-02 You're viewing this 1 CONTAINER in 1 CARTON (72220-002-02) / 20 g in 1 CONTAINER (72220-002-01) 2024-11-01 Active
72220-0002-04 1 CONTAINER in 1 CARTON (72220-002-04) / 20 g in 1 CONTAINER (72220-002-03) 2024-11-01 Active

Pack size FAQ

What quantity is in NDC 72220-0002-02?
NDC 72220-0002-02 contains 20 g — 1 container in 1 carton / 20 g in 1 container.
What is the difference between NDC 72220-0002-02 and NDC 72220-0002-04?
Both are MDP PEPTIDE 9 BIO SUN PRO Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane 9.5 g/100g; 5 g/100g; 2.7 g/100g; 4.5 g/100g Stick — the drug itself is identical. NDC 72220-0002-02 is the 20 g package, while NDC 72220-0002-04 is the 20 g package.
What NDC number is used to bill for this package of MDP PEPTIDE 9 BIO SUN PRO Homosalate, Octocrylene, Ethylhexyl Salicylate, Butyl Methoxydibenzoylmethane 9.5 g/100g; 5 g/100g; 2.7 g/100g; 4.5 g/100g Stick?
Bill NDC 72220-0002-02 — the 11-digit billing format is 72220000202. 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 72220-002-02, 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: 72220-0002-02, written without dashes as 72220000202. 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 72220-0002-02, the first segment (72220) is the labeler code FDA assigned to SKINIDEA CO., LTD; the middle segment (0002) 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 SKINIDEA CO., 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 20 g (72220-0002-04). 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?
SKINIDEA 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.

📄 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 📋 Description
🎯 Indications and Usage 31 words ▾

Use(s) ■ 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 104 words ▾

Directions For sunscreen use: • Apply liberally and evenly 15 minutes before sun exposure • Children under 6 months of age: Ask a doctor • Reapply at least every 2 hours • Use a water-resistant sunscreen if swimming or sweating • 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 57 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 swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 10 words ▾

Active ingredients Avobenzone 2.70% Homosalate 9.50% Octisalate 4.50% Octocrylene 5.00%

🧪 Inactive Ingredients 182 words ▾

Inactive ingredients Dimethicone, Methyl Methacrylate Crosspolymer, Synthetic Wax, Diethylhexyl Carbonate, Diisopropyl Sebacate, Diphenylsiloxy Phenyl Trimethicone, Isopropyl Palmitate, Polymethyl Methacrylate, Caprylyl Trimethicone, Diisostearyl Malate, Phenethyl Benzoate, Acrylates Copolymer, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyloctyl Salicylate, Polyethylene, Dimethicone/Vinyl Dimethicone Crosspolymer, Curcuma Longa (Turmeric) Root Extract, Camellia Japonica Seed Oil, Melia Azadirachta Flower Extract, Melia Azadirachta Leaf Extract, Corallina Officinalis Extract, Melia Azadirachta Bark Extract, Moringa Oleifera Seed Oil, Ocimum Sanctum Leaf Extract, Hydrolyzed Hyaluronic Acid, Collagen Amino Acids, Haematococcus Pluvialis Extract, Collagen, Aloe Barbadensis Leaf Extract, Dioscorea Japonica Root Extract, Laminaria Japonica Extract, Sodium Hyaluronate, Ulmus Davidiana Root Extract, Viola Mandshurica Flower Extract, Heptasodium Hexacarboxymethyl Dipeptide-12, Anemarrhena Asphodeloides Root Extract, Hyaluronic Acid, Collagen Extract, Microcrystalline Wax, Polymethylsilsesquioxane, Ethylene/Propylene Copolymer, Silica Dimethyl Silylate, Dimethicone Crosspolymer, Water, Butylene Glycol, Ectoin, Ubiquinone, Hydrogenated Polyisobutene, Glycerin, 1,2-Hexanediol, Propanediol, Sorbitan Laurate, Hydroxyethylcellulose, Acetyl Dipeptide-1 Cetyl Ester, Hydroxypropyltrimonium Hyaluronate, Acetyl Hexapeptide-8, Ascorbic Acid Polypeptide, Dextran, Hexapeptide-9, Sodium Acetylated Hyaluronate, Tripeptide-1, Tocopherol, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, Acetyl Octapeptide-3, Acetyl Tetrapeptide-2, Acetyl Tetrapeptide-3, Acetyl Tetrapeptide-5, Acetyl Tetrapeptide-9, Carnosine, Copper Tripeptide-1, Nonapeptide-1, Palmitoyl Pentapeptide-4, Palmitoyl Tripeptide-1, Palmitoyl Tripeptide-5, Fragrance

🎯 Purpose 2 words ▾

Purpose Sunscreen

📋 Description 26 words ▾

Other Information ■ Protect the product in this container from excessive heat and direct sun Questions? ■ Please send an email to the following address [email protected]

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 72208-0530-01 · Deciem 72220-0003-02 · SKINIDEA →
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.