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Sun Juice Body Mist Sunscreen SPF30 - Vanilla Breeze PARADISO Avobenzone, Homosalate, Octisalate 75 mg/mL; 30 mg/mL; 50 mg/mL Spray, 60 mL — NDC 84130-0023-20 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Sun Juice Body Mist Sunscreen SPF30 - Vanilla Breeze PARADISO Avobenzone, Homosalate, Octisalate 75 mg/mL; 30 mg/mL; 50 mg/mL Spray, 60 mL — NDC 84130-023-20 (Billing 84130-0023-20)

by Koco Life LLC · 60 mL in 1 BOTTLE, PUMP

This is a package of 60 mL of Sun Juice Body Mist Sunscreen SPF30 - Vanilla Breeze PARADISO Avobenzone, Homosalate, Octisalate 75 mg/mL; 30 mg/mL; 50 mg/mL Spray from Koco Life LLC, marketed since Dec 2025 and currently FDA-listed. It is this product's only package size.

NDC 84130-0023-20
🏷️ FDA NDC (as labeled) 84130-023-20 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 84130-023-20 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84130 labeler · 023 product · 20 package
Package marketed since
Dec 1, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8413002320 8
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84130-023-20
Product NDC 84130-023
11-digit billing NDC 84130002320
UNII V06SV4M95S, G63QQF2NOX, 4X49Y0596W
Application # M020
SPL Set ID 3cc62c97-70c5-17f7-e063-6394a90abe25
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-12-01
Route TOPICAL
Dosage form SPRAY
Substance HOMOSALATE; AVOBENZONE; OCTISALATE
Why two NDCs? The FDA registers this code as 84130-023-20 — 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 → 84130-0023-20. 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?

Sun Juice Body Mist Sunscreen SPF30 is a topical spray sunscreen marketed as an over-the-counter monograph product. It contains three active ingredients, avobenzone, homosalate, and octisalate, which are ultraviolet light absorbers commonly used together in sunscreen formulations to help protect skin from sun exposure. This product is applied directly to the skin as a spray mist.

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 mLPer 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
84130-0023-20 You're viewing this Main listing 60 mL in 1 BOTTLE, PUMP 2025-12-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Sun Juice Body Mist Sunscreen SPF30 - Coconut Cream PARADISO 75 mg/mL; 30 mg/mL; 50 mg/mL 84130-0022-20 Koco 60 ml — — FDA listed —
Sun Juice Body Mist Sunscreen SPF30 - Vanilla Breeze PARADISO 75 mg/mL; 30 mg/mL; 50 mg/mLthis 84130-0023-20 Koco 60 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

🏛️
2025
On the market since
Dec 2025
📍
2026
Currently FDA-listed
1 year 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 2EH13UN8D3
    A synthetic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and allows them to penetrate the skin more effectively.
  • UNII A4VZ22K1WT
    Coumarin is a fragrant organic compound derived from plants or made synthetically. It adds pleasant flavor and aroma to medicines and is used as a flavoring agent in some formulations.
  • UNII 4X371TMK9K
    Dibutyl maleate is a synthetic chemical compound used as a plasticizer and solvent in pharmaceutical formulations. It helps soften and improve the flexibility of coatings and film-forming ingredients in medicines.
  • UNII 28N247O58B
    A synthetic alcohol used as a solvent and preservative in liquid medicines. It helps dissolve active ingredients and prevents microbial growth in the formulation.
  • UNII IX0PRH184P
    A synthetic compound made from borneol and acrylic acid, used as a film-forming agent and binder in pharmaceutical coatings and adhesive formulations to help create protective layers on tablets or control drug release.
  • UNII R60QEP13IC
    Rice bran is a natural powder made from the outer layer of rice grains. It's used in medicines as a filler and flow agent to add bulk and help the product mix and flow smoothly during manufacturing.
  • UNII F3IN55X5PO
    A plant-derived essential oil from patchouli leaves. It serves as a fragrance and flavoring agent to improve the taste and smell of the medicine.
  • UNII T9296U138P
    A synthetic polymer derived from polyester chemistry, modified with a cyanodiphenylpropenoyl cap. It serves as a film-former and binder in pharmaceutical formulations, helping create protective coatings on tablets or improving product consistency.
  • UNII 2JU6ZH6GRE
    A synthetic fragrance compound made by modifying naphthalene molecules. It's used in very small amounts to add pleasant scent to medications, making them more appealing to take.
  • UNII CHI530446X
    Vanillin is a natural or synthetic aromatic compound that gives vanilla flavor. It's used in medicines as a flavoring agent to mask bitter tastes and improve how the medicine tastes.
  • UNII YA7T88HHM8
    Vinyl acrylate is a synthetic polymer used as a film-coating agent on tablets and capsules. It helps protect the medicine and control how quickly the active ingredient is released in the body.

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

The official label also statesAlcohol Denat., VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Oryza Sativa (Rice) Bran Oil, Butyloctyl Salicylate, Polyester-8, Fragrance (Parfum), Coumarin, Tetramethyl Acetyloctahydronaphthalenes, Vanillin, Pogostemon Cablin Oil, Trimethylcyclopentenyl Methylisopentenol

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.

Manufacturer & labeler

LabelerKoco Life LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code84130
First marketedDec 2025
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 29 words ▾

Uses Helps prevent sunburn If used as directed with other sun protection measures (see Directions), decreass the risk of skin cancer & early skin aging caused by the sun

⏱️ Dosage and Administration 128 words ▾

Directions Spritz generously and evenly onto clean, dry skin 15 minutes before sun exposure for instant sun protection and a radiant glow. Layer with your favorite scents for a sunkissed signature. For Sunscreen use: Apply generously and evenly 15 minutes before sun exposure.

Reapply After 80 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 & early skin aging.

To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher & 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 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 14 words ▾

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

🧪 Active Ingredient 8 words ▾

Active ingredients Avobenzone 3%, Homosalate 7.5%, Octisalate 5%

🧪 Inactive Ingredients 27 words ▾

Inactive ingredients Alcohol Denat., VA/Butyl Maleate/Isobornyl Acrylate Copolymer, Oryza Sativa (Rice) Bran Oil, Butyloctyl Salicylate, Polyester-8, Fragrance (Parfum), Coumarin, Tetramethyl Acetyloctahydronaphthalenes, Vanillin, Pogostemon Cablin Oil, Trimethylcyclopentenyl Methylisopentenol

🎯 Purpose 7 words ▾

Purpose Avobenzone 3%, Homosalate 7.5%, 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 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 4 words ▾

Questions/Comments Call (858) 252-0099

📄 Package Label / Principal Display Panel 27 words ▾

Kopari Paradiso SPF 30 Sun Juice Body Mist Sunscreen Broad Spectrum SPF 30 Water Resistant (80 Minutes) Vanilla Breeze 2 Fl. Oz. | 60 mL 1 2

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

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 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.
← 84130-0022-20 · Koco 84130-0024-96 · 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.