Home › NDC Lookup › Ingredients › Avobenzone, Homosalate, Octocrylene, Oct... › 84130-0008-99
Sun Essentials SPF Duo Kit Avobenzone, Homosalate, Octocrylene, Octisalate Kit — NDC 84130-0008-99 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Sun Essentials SPF Duo Kit Avobenzone, Homosalate, Octocrylene, Octisalate Kit — NDC 84130-008-99 (Billing 84130-0008-99)

by Koco Life LLC · 1 KIT in 1 KIT * 30 mL in 1 BOTTLE, PUMP * 150 mL in 1 BOTTLE, PUMP

This is a package of Sun Essentials SPF Duo Kit Avobenzone, Homosalate, Octocrylene, Octisalate Kit from Koco Life LLC, marketed since Jun 2024 and currently FDA-listed. It is this product's only package size.

NDC 84130-0008-99
🏷️ FDA NDC (as labeled) 84130-008-99 billing pads the product segment with a zero
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 84130-008-99 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84130 labeler · 008 product · 99 package
Package marketed since
Jun 28, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0850056558099
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84130-008-99
Product NDC 84130-008
11-digit billing NDC 84130000899
UPC 0850056558099
Application # M020
SPL Set ID 1c329b86-664e-de1f-e063-6394a90a7c23
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-06-28
Route TOPICAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 84130-008-99 — 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 → 84130-0008-99. 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 sunscreen kit containing multiple UV-filtering ingredients commonly used to protect skin from sun damage. Avobenzone, homosalate, octocrylene, and octisalate are organic compounds that function as ultraviolet absorbers, typically used together in sunscreen formulations to provide broad-spectrum protection against both UVA and UVB radiation. The kit format allows consumers to apply the sunscreen product to exposed skin as part of daily sun protection routines. This is an over-the-counter monograph drug marketed under FDA's established rules for sunscreen products.

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
84130-0008-99 You're viewing this Main listing 1 KIT in 1 KIT * 30 mL in 1 BOTTLE, PUMP * 150 mL in 1 BOTTLE, PUMP 2024-06-28 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
REDEFINE Triple Defense .02 g/mL; .068 g/mL; .044 g/mL; .034 g/mL 14222-2252-01 Rodan 1 bottle — — FDA listed —
Aruba Aloe broad spectrum SPF 15 Lip sunscreen and Moisturizer 30 mg/g; 73.4 mg/g; 50 mg/g; 50 mg/g 53675-0208-00 Aruba 4.8 g — — FDA listed —
SPF30 Sunscreen 30 mg/g; 100 mg/g; 100 mg/g; 50 mg/g 70412-0211-15 Zhejiang 15 g — — FDA listed —
SPF15 Sunscreen 20 mg/g; 80 mg/g; 55 mg/g; 20 mg/g 70412-0212-02 Zhejiang 2 g — — FDA listed —
SPF 15 Lip and SPF 30 Sunscreen 70412-0819-10 Zhejiang 1 kit — — FDA listed —
SPF 30 Sunscreen 30 mg/mL; 100 mg/mL; 100 mg/mL; 50 mg/mL 71160-0331-30 Tekweld 1 bottle — — FDA listed —
SPF 30 Sunscreen 30 mg/mL; 100 mg/mL; 100 mg/mL; 50 mg/mL 71160-0338-10 Tekweld 1 bottle — — FDA listed —
ALLIES OF SKIN The One SPF-50 Invisible Sunscreen 30 mg/mL; 70 mg/mL; 100 mg/mL; 50 mg/mL 83852-0438-03 ALLIES 3 ml — — FDA listed —
SPF30 unseen sunscreen stick 01 3 g/100g; 10 g/100g; 10 g/100g; 5 g/100g 82953-0047-01 Cosmuses 10 g — — FDA listed —
Sunscreen SPF 30 30 mg/mL; 100 mg/mL; 100 mg/mL; 50 mg/mL 80524-0002-30 Tempo 30 ml — — FDA listed —
Curology Daily Moisturizing 4 g/100mL; 5 g/100mL; 6 g/100mL; 1.5 g/100mL 82575-0400-00 Curology, 1 tube — — FDA listed —
Rose Gold Sun Shield Body Glow SPF45 50 mg/mL; 100 mg/mL; 30 mg/mL; 100 mg/mL 84130-0002-50 Koco 150 ml — — FDA listed —
Sun on the Run Kit 84130-0009-98 Koco 1 kit — — FDA listed —
Spf15 20 mg/g; 80 mg/g; 55 mg/g; 20 mg/g 70412-0316-07 Zhejiang 2 g — — FDA listed —
Sun Shield On-the-Glow Sheer Stick SPF40 10 g/100g; 5 g/100g; 3 g/100g; 10 g/100g 84130-0004-10 Koco 30 g — — FDA listed —
Sun Voyage Kit 84130-0013-97 Koco 1 kit — — FDA listed —
5281 Sunscreen 30 mg/mL; 100 mg/mL; 100 mg/mL; 50 mg/mL 76138-0219-05 Innovation 15 ml — — FDA listed —
Eva Claire Natural Professional Sunscreen 4.35 g/50mL; 3.65 g/50mL; .7 g/50mL; 2.4 g/50mL 87364-0100-02 Eva 1 tube — — FDA listed —
REVERSE Brightening Defense Fluid .028 g/mL; .093 g/mL; .061 g/mL; .0467 g/mL 14222-2300-01 Rodan 1 tube — — FDA listed —
5298 Sunscreen 30 mg/mL; 100 mg/mL; 100 mg/mL; 50 mg/mL 76138-0220-02 Innovation 60 ml — — FDA listed —
5299 Sunscreen 30 mg/mL; 100 mg/mL; 100 mg/mL; 50 mg/mL 76138-0221-06 Innovation 20 ml — — FDA listed —
Sun Essentials SPF Duo Kitthis 84130-0008-99 Koco 1 kit — — FDA listed —
Dr. Idriss Major Fade Disco Block Whipped Sunscreen SPF 50 5 g/100mL; 10 g/100mL; 3 g/100mL; 7 g/100mL 85246-0100-01 PILLOWTALKDERM 1 tube — — FDA listed —
Aruba Aloe Hydrating Aloe Rich Sunscreen SPF 50 30 mg/mL; 73.4 mg/mL; 100 mg/mL; 50 mg/mL 53675-0210-01 Aruba 59 ml — — FDA listed —
Aruba Aloe Hydrating Aloe Rich Sunscreen SPF 30 30 mg/mL; 73.4 mg/mL; 100 mg/mL; 50 mg/mL 53675-0211-01 Aruba 59 ml — — FDA listed —
5407 Sunscreen 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL 76138-0223-01 Innovation 30 ml — — FDA listed —
Aruba Aloe Hydrating Aloe Rich Sunscreen SPF 15 30 mg/mL; 73.4 mg/mL; 50 mg/mL; 50 mg/mL 53675-0214-00 Aruba 177 ml — — FDA listed —
5283 Sunscreen 3 g/100mL; 10 g/100mL; 10 g/100mL; 5 g/100mL 76138-0222-01 Innovation 30 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

🏛️
2024
On the market since
Jun 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.

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.

From the label’s inactive-ingredient sectionOctyldodecanol, C12-15 Alkyl Benzoate, Polyamide-3, Butyloctyl Salicylate, Octyldodecyl Neopentanoate, Fragrance (Parfum), Persea Gratissima (Avocado) Oil, Hibiscus Sabdariffa Seed Oil, Cocos Nucifera (Coconut) Oil, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Aleurites Moluccana Seed Oil, Tocopheryl Acetate, Macadamia Ternifolia Seed Oil, Benzyl Salicylate, Hexyl Cinnamal, Linalool, Mica (CI 77019), Titanium Dioxide (CI 77891), Iron Oxides (CI 77491).

This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.

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

LabelerKoco Life LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code84130
First marketedJun 2024
Product typeHuman Otc Drug
Portfolio27 products on file

More NDCs from Koco Life LLC labeler code 84130

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 28 words ▾

Uses • Helps prevent sunburn • If used as directed with other sunprotection measures (see Directions),decreases the risk of skin cancer and earlyskin aging caused by the sun

⏱️ Dosage and Administration 98 words ▾

Directions • Apply generously & evenly 15 minutesbefore sun exposure. REAPPLY: After 40 minutes of swimming or sweating. • Immediately after towel drying.• 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 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 • Children under 6 months: Ask a doctor

⚠️ Warnings 58 words ▾

Warnings For e xternal 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 14 words ▾

Other information Protect the product in this container from excessive heat and direct sun

🧪 Active Ingredient 10 words ▾

Active ingredients Avobenzone 3% Homosalate 10% Octocrylene 10% Octisalate 5%

🧪 Inactive Ingredients 54 words ▾

Inactive ingredients Octyldodecanol, C12-15 Alkyl Benzoate, Polyamide-3, Butyloctyl Salicylate, Octyldodecyl Neopentanoate, Fragrance (Parfum), Persea Gratissima (Avocado) Oil, Hibiscus Sabdariffa Seed Oil, Cocos Nucifera (Coconut) Oil, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Aleurites Moluccana Seed Oil, Tocopheryl Acetate, Macadamia Ternifolia Seed Oil, Benzyl Salicylate, Hexyl Cinnamal, Linalool, Mica (CI 77019), Titanium Dioxide (CI 77891), Iron Oxides (CI 77491).

🎯 Purpose 9 words ▾

Purpose Avobenzone 3%.....................Sunscreen Homosalate 10%....................Sunscreen Octocrylene 10%....................Sunscreen Octisalate 5%.........................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 22 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 (858) 252-0099

📄 Package Label / Principal Display Panel 17 words ▾

Kopari Sun Shield Body Glow Sunscreen SPF 50 DUO Endless Glow, Applies Clear, Absorbs Seamlessly 1 2

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, Octocrylene, Octisalate — the ingredient across all brands.

Top reported reactions

Rash14
Erythema11
Acne10
Dry Skin10
Sunburn9
Malignant Melanoma8
Condition Aggravated7

Reporter sex

146 reports

Serious outcomes

Hospitalization22
Disabling3
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 14 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

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 ✓ 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 Koco Life LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Koco Life LLC 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.
← 84130-0007-12 · Koco 84130-0009-98 · Koco →
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.