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Glow This Way Octisalate, Octocrylene, Zinc Oxide, Avobenzone, Homosalate Kit — NDC 84130-0025-95 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Glow This Way Octisalate, Octocrylene, Zinc Oxide, Avobenzone, Homosalate Kit — NDC 84130-025-95 (Billing 84130-0025-95)

by Koco Life LLC · 1 KIT in 1 KIT * 1 TUBE in 1 CARTON / 15 g in 1 TUBE * 30 mL in 1 BOTTLE, DROPPER * 40 mL in 1 BOTTLE, PUMP

This is a package of Glow This Way Octisalate, Octocrylene, Zinc Oxide, Avobenzone, Homosalate Kit from Koco Life LLC, marketed since Dec 2025 and currently FDA-listed. It is this product's only package size.

NDC 84130-0025-95
🏷️ FDA NDC (as labeled) 84130-025-95 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 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 84130-025-95 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84130 labeler · 025 product · 95 package
Package marketed since
Dec 12, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8413002595 0
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84130-025-95
Product NDC 84130-025
11-digit billing NDC 84130002595
Application # M020
SPL Set ID 4619cf96-987a-3e88-e063-6294a90afbe9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-12-12
Route TOPICAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 84130-025-95 — 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 → 84130-0025-95. 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 five UV-filtering ingredients. Octisalate, octocrylene, homosalate, and avobenzone are organic UV absorbers that help protect skin from ultraviolet radiation. Zinc oxide is a mineral UV reflectant that works similarly. These ingredients are typically combined in over-the-counter sunscreen products to provide broad-spectrum UV protection when applied to exposed skin.

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
84130-0025-95 You're viewing this Main listing 1 KIT in 1 KIT * 1 TUBE in 1 CARTON / 15 g in 1 TUBE * 30 mL in 1 BOTTLE, DROPPER * 40 mL in 1 BOTTLE, PUMP 2025-12-12 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Glow This Waythis 84130-0025-95 Koco 1 kit — — 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.

From the label’s inactive-ingredient sectionAlcohol Denat., Butyloctyl Salicylate, Diisopropyl Adipate, Lauryl Lactate, Dicaprylyl Carbonate, Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Tetrahexyldecyl Ascorbate, Tocopherol, Citrus Aurantifolia (Lime) Oil, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantium Peel Oil, Hydrogenated Castor Oil, Oryza Sativa (Rice) Bran Extract, Communis (Castor) Seed Oil, Glycerin, Triethyl Citrate, Gamma Decalactone, Maltol, Dimethyl Heptenal, Hexyl Acetate, Ethyl Butyrate, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, t-Butyl Alcohol, Mica, Water/Aqua/Eau, Propanediol, Polyglutamic Acid, Citric Acid, Sodium Benzoate, Limonene, Geraniol, Geranyl Acetate, Terpineol, 3,6-Nonadienol, Tin Oxide, CI 77891 (Titanium DIoxide), CI 77491 (Iron Oxides). Octyldodecanol, Hydrogenated Polyisobutene, Diisostearyl Malate, C15-19 Alkane, Phytosteryl/Isostearyl/Cetyl/Stearyl/Behenyl Dimer Dilinoleate, Hydrogenated Styrene/Isoprene Copolymer, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Water/Aqua/Eau, Polyglyceryl-4 Isostearate, Quaternium-90 Bentonite, Squalane, Flavor (Aroma), Cocos Nucifera (Coconut) Fruit Extract, Polyhydroxystearic Acid, Triethyl Citrate, Isostearyl Alcohol, 1,2-Hexanediol, Caprylyl Glycol, Ethyl Ferulate, Glycerin, Pentaerythrityl Tetra-Di-t-Butyl Hydroxyhydrocinnamate, Tocopheryl Acetate, Maltodextrin, Phytosteryl/Octyldodecyl Lauroyl Glutamate, Simmondsia Chinensis (Jojoba) Seed Oil, Malic Acid, C10-18 Triglycerides, Sodium Hyaluronate, Ceramide NP, Hydrogenated Lecithin, Punica Granatum Flower Extract, Triolein, Polyglyceryl-3 Diisostearate, Glyceryl Dioleate, Tocopherol, Sorbitan Oleate, Benzyl Alcohol, Vanillin, Iron Oxides (CI 77491, CI 77492, CI 77499) Water/Aqua/Eau, Butyloctyl Salicylate, Polyglyceryl-3 Polyricinoleate, Propanediol, Sodium Chloride, Caprylic/Capric Triglyceride, Mica, Niacinamide, Sodium Hyaluronate, Panthenol, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantifolia (Lime) Oil, Tocopherol, 1,2-Hexanediol, Styrene/MA Copolymer, Ethylhexylglycerin, Triethyl Citrate, Xanthan Gum, Maltol, Dimethyl Heptenal, Gamma-Decalactone, Geraniol, Geranyl Acetate, 3,6-Nonadienol, Terpineol, Hexyl Acetate, Ethyl Butyrate, Benzyl Alcohol, Limonene, Citrus Aurantium Peel Oil, Sodium Hydroxide, Tin Oxide, Sodium Ferrocyanide, Iron Titanium Oxide, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

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 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 87 words ▾

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

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

Uses 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 ~1 min read ▾

Directions Shake well before use. With eyes closed, spray generously and evenlyover your face while holding spray 8-10 inches away. Apply 15 minutesbefore sun exposure. • Reapply: After 40 minutes of swimming orsweating. • Immediately after towel drying. • At least every 2 hours.

Do notspray directly into eyes • Sun Protection Measures Spending time in thesun increases your risk of skin cancer & early skin aging. To decrease thisrisk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 orhigher & other sun protection measures including: • Limit time in the sun,especially from 10 a.m. - 2 p.m. • Wear long-sleeved shirts, hats, andsunglasses • Children under 6 months of age: Ask a doctor

Directions • Apply generously & evenly 15 minutes before sun exposure. REAPPLY : 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. • Wearlong-sleeved shirts, pants, hats, and sunglasses • Children under 6 months: Ask a doctor

Directions Apply generously & evenly 15 minutes before sun exposure 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 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 doctor

⚠️ Warnings 165 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 a rash occurs. ● Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

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

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. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 44 words ▾

Other information • Protect this product fromexcessive heat and direct sun • May stain some fabrics

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

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

🧪 Active Ingredient 24 words ▾

Active ingredients Avobenzone 3%, Homosalate 0.5%, Octisalate 5%, Octyocrylene 10%

Active ingredient Zinc Oxide 10.88%

Active ingredients Octisalate 5% Octocrylene 10% Zinc Oxide 15%

🧪 Inactive Ingredients ~1 min read ▾

Inactive ingredients Alcohol Denat., Butyloctyl Salicylate, Diisopropyl Adipate, Lauryl Lactate, Dicaprylyl Carbonate, Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Tetrahexyldecyl Ascorbate, Tocopherol, Citrus Aurantifolia (Lime) Oil, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantium Peel Oil, Hydrogenated Castor Oil, Oryza Sativa (Rice) Bran Extract, Communis (Castor) Seed Oil, Glycerin, Triethyl Citrate, Gamma Decalactone, Maltol, Dimethyl Heptenal, Hexyl Acetate, Ethyl Butyrate, VA/Butyl Maleate/Isobornyl Acrylate Copolymer, t-Butyl Alcohol, Mica, Water/Aqua/Eau, Propanediol, Polyglutamic Acid, Citric Acid, Sodium Benzoate, Limonene, Geraniol, Geranyl Acetate, Terpineol, 3,6-Nonadienol, Tin Oxide, CI 77891 (Titanium DIoxide), CI 77491 (Iron Oxides).

Inactive ingredients Octyldodecanol, Hydrogenated Polyisobutene, Diisostearyl Malate, C15-19 Alkane, Phytosteryl/Isostearyl/Cetyl/Stearyl/Behenyl Dimer Dilinoleate, Hydrogenated Styrene/Isoprene Copolymer, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Water/Aqua/Eau, Polyglyceryl-4 Isostearate, Quaternium-90 Bentonite, Squalane, Flavor (Aroma), Cocos Nucifera (Coconut) Fruit Extract, Polyhydroxystearic Acid, Triethyl Citrate, Isostearyl Alcohol, 1,2-Hexanediol, Caprylyl Glycol, Ethyl Ferulate, Glycerin, Pentaerythrityl Tetra-Di-t-Butyl Hydroxyhydrocinnamate, Tocopheryl Acetate, Maltodextrin, Phytosteryl/Octyldodecyl Lauroyl Glutamate, Simmondsia Chinensis (Jojoba) Seed Oil, Malic Acid, C10-18 Triglycerides, Sodium Hyaluronate, Ceramide NP, Hydrogenated Lecithin, Punica Granatum Flower Extract, Triolein, Polyglyceryl-3 Diisostearate, Glyceryl Dioleate, Tocopherol, Sorbitan Oleate, Benzyl Alcohol, Vanillin, Iron Oxides (CI 77491, CI 77492, CI 77499)

Inactive ingredients Water/Aqua/Eau, Butyloctyl Salicylate, Polyglyceryl-3 Polyricinoleate, Propanediol, Sodium Chloride, Caprylic/Capric Triglyceride, Mica, Niacinamide, Sodium Hyaluronate, Panthenol, Litsea Cubeba Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Mentha Viridis (Spearmint) Leaf Oil, Citrus Aurantifolia (Lime) Oil, Tocopherol, 1,2-Hexanediol, Styrene/MA Copolymer, Ethylhexylglycerin, Triethyl Citrate, Xanthan Gum, Maltol, Dimethyl Heptenal, Gamma-Decalactone, Geraniol, Geranyl Acetate, 3,6-Nonadienol, Terpineol, Hexyl Acetate, Ethyl Butyrate, Benzyl Alcohol, Limonene, Citrus Aurantium Peel Oil, Sodium Hydroxide, Tin Oxide, Sodium Ferrocyanide, Iron Titanium Oxide, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

🎯 Purpose 21 words ▾

Purpose Avobenzone 3%, Homosalate 0.5%, Octisalate 5%, Octyocrylene 10%.................Sunscreen

Purpose Zinc Oxide 10.88%...Sunscreen

Purpose Octisalate 5%.................Sunscreen Octocrylene 10%.................Sunscreen Zinc Oxide 15%.................Sunscreen

📄 Do Not Use 25 words ▾

● Do not use on damage or broken skin

Do not use on damaged or broken skin

Do not use on damaged or broken skin

📄 When Using This Product 40 words ▾

● When using this product keep out of eyes. Rinse with water to remove.

When using this product keep out of eyes Rinse with water to remove

When using this product keep out of eyes. Rinse with water to remove.

📄 Stop Use and Ask a Doctor If 20 words ▾

● Stop use and ask a doctor if a rash occurs.

Stop use and ask a doctor if rash occurs

📄 Keep Out of Reach of Children 65 words ▾

● Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children If product is swallowed , get medical help or contact a Poison Control Center right away

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 16 words ▾

Questions/Comments Call (858) 252-0099

Questions or comments? Call (858) 252-0099

Questions or comments? Call (858) 252-0099

📄 Package Label / Principal Display Panel 5 words ▾

Kopari Glow This Way 1

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 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.
← 84130-0024-96 · Koco 84130-0026-20 · 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.