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Abib No White Cast SPF Gift Set homosalate, octocrylene,octisalate,avobenzone Kit

by FOURCOMPANY CO., LTD. · 1 KIT in 1 BOX (73676-416-40) * 22 g in 1 CONTAINER (73676-216-20) * 23 g in 1 CONTAINER (73676-116-20) * 50 mL in 1 TUBE (73676-200-01) * 30 mL in 1 TUBE (73676-100-01)
NDC 73676-0416-40
🏷️ FDA NDC (as labeled) 73676-416-40 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 73676-416-40
Product NDC 73676-416
11-digit billing NDC 73676041640
Application # M020
SPL Set ID 537420bb-9fd8-0649-e063-6394a90aa8cf
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-26
Route TOPICAL
Dosage form KIT
Why two NDCs? The FDA registers this code as 73676-416-40 — 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 → 73676-0416-40. 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

LabelerFOURCOMPANY CO., LTD.
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code73676
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio10 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?

This kit contains a topical sunscreen product marketed under FDA's over-the-counter monograph rules. The active ingredients are homosalate, octocrylene, octisalate, and avobenzone, which are ultraviolet light filters commonly used together in sunscreen formulations to help protect skin from sun exposure. These chemical filters work by absorbing UV radiation. The product is intended for topical application to the 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.

🧪 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, Butylene Glycol Dicaprylate/Dicaprate, Dibutyl Lauroyl Glutamide, Diisostearyl Malate, Dibutyl Ethylhexanoyl Glutamide, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Dextrin Palmitate, Water, Sodium Hyaluronate, Squalane, Calophyllum Inophyllum Seed Oil, Argania Spinosa Kegnel Oil, Olea Euro paea (Olive) Fruit Oil, Glycerin, Aloe Barbadensis Leaf Extract, Hydrolyzed Vegetable Protein, Maltodextrin, Butylene Glycol, Propanediol, Caprylic/Capric Trigly ceride, 1,2-Hexanediol, Camellia Sinensis Leaf Extract, Hydrogenated Lecithin, Centella Asiatica Extract, Candida Bombicola/Glucose/Methyl Rapeseedate Fer ment, Ceramide NP, Caprylyl Glycol, Tocopherol, Acetyl Hexapeptide-8, Copper Tripeptide-1 Dimethicone, Synthetic Wax, Silica, Isoeicosane, Phenylpropy ldimethylsiloxy silicate, Isopropyl Palmitate, Disostearyl Malate, Butylocty/ Salicylate, Isononyl Isononanoate, Phenethyl Benzoate, Diethylhexyl Carbonate, Hydrogenated Vegetable Oil, Synthetic Fluorphlogopite, Polyethylene, Dimethicone Crosspolymer, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Ethylene/Propylene Copolymer, Camellia Japonica Seed Oil,Copernicia Cerifera (Carnauba) Wax, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Silica Dimethyl Silylate, Euphorbia Cerifera (Candelilla) Wax, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Allantoin, Ectoin Water, Butylene Glycol, Acrylates Copolymer, Benzotriazolyl Dodecyl p-Cresol, Alcohol Denat., Methyl Methacrylate Crosspolymer, Pentylene Glycol, Cetyl Alcohol, 1,2-Hexanediol, Hydroxyacetophenone, Silica Dimethyl Silylate, Polyacrylic Acid, Chamaecyparis Obtusa Oil, Tromethamine, Ammonium Acryloyldimethyltaurate/VP Copolymer, Polyamide-8, Hydroxypropyl Methylcellulose, Butylene Glycol Dicaprylate/Dicaprate, Hydroxypropyl Methylcellulose Stearoxy Ether, Rosmarinus Officinalis (Rosemary) Leaf Oil, Xanthan Gum, Cynanchum Atratum Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Ethylhexylglycerin, Althaea Rosea Flower Extract, Ascorbic Acid, Ascorbyl Glucoside, Niacinamide, Hyaluronic Acid, Hydrolyzed Hyaluronic Acid, Collagen Extract, Sodium Hyaluronate Isododecane, Butyloctyl Salicylate, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Dextrin Palmitate, Dibutyl Adipate, Methyl Methacrylate Crosspolymer, Acrylates Copolymer, Benzotriazolyl Dodecyl p-Cresol, Polyphenylsilsesquioxane, Trimethylsiloxysilicate, Cedrus Atlantica Bark Oil, Tocopherol, Cananga Odorata Flower Oil, Glycerin, Squalane, Tocopheryl Acetate, Jasminum Officinale (Jasmine) Oil, Ectoin, Sodium Hyaluronate

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Abib Quick And Airy Sunstick Duo Set 73676-0316-40 FOURCOMPANY 1 kit — — FDA listed —
Abib No White Cast SPF Gift Setthis 73676-0416-40 FOURCOMPANY 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
Jun 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
73676-0416-40 You're viewing this 1 KIT in 1 BOX (73676-416-40) * 22 g in 1 CONTAINER (73676-216-20) * 23 g in 1 CONTAINER (73676-116-20) * 50 mL in 1 TUBE (73676-200-01) * 30 mL in 1 TUBE (73676-100-01) 2026-06-26 Active

🧭 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 — Not published for this NDC No photo available yet for this listing.
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 73676-416-40, 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: 73676-0416-40, written without dashes as 73676041640. 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 73676-0416-40, the first segment (73676) is the labeler code FDA assigned to FOURCOMPANY CO., LTD.; the middle segment (0416) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (40) 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 FOURCOMPANY CO., LTD.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
FOURCOMPANY 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
🎯 Indications and Usage 126 words ▾

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

Uses help prevent sunburn if used as directed with other sun protection measures ( see Directions ), deacreases the risk of skin cancer and early skin 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

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 ~2 min read ▾

Directions apply liberally and evenly 15 minutes before sun exposure. children under 6 months of age: ask a doctor. Sun protection measures: spending time in the sun increases your risk of skin cancer and early 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

Directions apply liberally and evenly 15 minutes before sun exposure. reapply: after 80 minutes of swimming or sweating. immediately after towel drying. at least every 2 hours. children under 6 months of age: ask a doctor. Sun protection measures . spending time in the sun increases your risk of skin cancer and early 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

Directions ■ Apply liberally and evenly 15 minutes before sun exposure. ■ Reapply at least every two 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 ■ Children under 6 months of age: Ask a doctor

Directions ■ Apply liberally and evenly 15 minutes before sun exposure. ■ Reapply at least every two 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 ■ Children under 6 months of age: Ask a doctor

⚠️ Warnings ~1 min read ▾

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 immediately.

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 immediately.

Warnings ■ For external use only. ■ Do not use on damaged or broken skin ■ Stop use and ask a doctor if rash occurs ■ When using this product keep out of eyes. Rinse with water to remove. ■ Keep out of reach of children. If 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 ■ Stop use and ask a doctor if rash occurs ■ When using this product keep out of eyes. Rinse with water to remove. ■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 38 words ▾

Active Ingredients Homosalate 9.50% Octocrylene 5.00% Octisalate 4.50% Avobenzone 3.00%.

Active ingredients Homosalate 9.50%, Octocrylene 5.00%, Octisalate 4.50%, Avobenzone 3.00%

Active ingredients Avobenzone 2.85%, Homosalate 13.50%, Octisalate 4.50%.

Active ingredients Avobenzone 2.80%, Homosalate 6.50%, Octisalate 4.50%, Octocrylene 8.00%

🧪 Inactive Ingredients ~1 min read ▾

Inactives ingredients Octyldodecanol, Butylene Glycol Dicaprylate/Dicaprate, Dibutyl Lauroyl Glutamide, Diisostearyl Malate, Dibutyl Ethylhexanoyl Glutamide, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Dextrin Palmitate, Water, Sodium Hyaluronate, Squalane, Calophyllum Inophyllum Seed Oil, Argania Spinosa Kegnel Oil, Olea Euro paea (Olive) Fruit Oil, Glycerin, Aloe Barbadensis Leaf Extract, Hydrolyzed Vegetable Protein, Maltodextrin, Butylene Glycol, Propanediol, Caprylic/Capric Trigly ceride, 1,2-Hexanediol, Camellia Sinensis Leaf Extract, Hydrogenated Lecithin, Centella Asiatica Extract, Candida Bombicola/Glucose/Methyl Rapeseedate Fer ment, Ceramide NP, Caprylyl Glycol, Tocopherol, Acetyl Hexapeptide-8, Copper Tripeptide-1

Inactive ingredients Dimethicone, Synthetic Wax, Silica, Isoeicosane, Phenylpropy ldimethylsiloxy silicate, Isopropyl Palmitate, Disostearyl Malate, Butylocty/ Salicylate, Isononyl Isononanoate, Phenethyl Benzoate, Diethylhexyl Carbonate, Hydrogenated Vegetable Oil, Synthetic Fluorphlogopite, Polyethylene, Dimethicone Crosspolymer, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Ethylene/Propylene Copolymer, Camellia Japonica Seed Oil,Copernicia Cerifera (Carnauba) Wax, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Silica Dimethyl Silylate, Euphorbia Cerifera (Candelilla) Wax, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Allantoin, Ectoin

Inactive ingredients Water, Butylene Glycol, Acrylates Copolymer, Benzotriazolyl Dodecyl p-Cresol, Alcohol Denat., Methyl Methacrylate Crosspolymer, Pentylene Glycol, Cetyl Alcohol, 1,2-Hexanediol, Hydroxyacetophenone, Silica Dimethyl Silylate, Polyacrylic Acid, Chamaecyparis Obtusa Oil, Tromethamine, Ammonium Acryloyldimethyltaurate/VP Copolymer, Polyamide-8, Hydroxypropyl Methylcellulose, Butylene Glycol Dicaprylate/Dicaprate, Hydroxypropyl Methylcellulose Stearoxy Ether, Rosmarinus Officinalis (Rosemary) Leaf Oil, Xanthan Gum, Cynanchum Atratum Extract, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Ethylhexylglycerin, Althaea Rosea Flower Extract, Ascorbic Acid, Ascorbyl Glucoside, Niacinamide, Hyaluronic Acid, Hydrolyzed Hyaluronic Acid, Collagen Extract, Sodium Hyaluronate

Inactive ingredients Isododecane, Butyloctyl Salicylate, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Dextrin Palmitate, Dibutyl Adipate, Methyl Methacrylate Crosspolymer, Acrylates Copolymer, Benzotriazolyl Dodecyl p-Cresol, Polyphenylsilsesquioxane, Trimethylsiloxysilicate, Cedrus Atlantica Bark Oil, Tocopherol, Cananga Odorata Flower Oil, Glycerin, Squalane, Tocopheryl Acetate, Jasminum Officinale (Jasmine) Oil, Ectoin, Sodium Hyaluronate

🎯 Purpose 8 words ▾

Purpose Sunscreen

Purpose Sunscreen

Purpose Sunscreen

Purpose Sunscreen

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 73676-0316-40 · FOURCOMPANY 73683-0101-10 · Nobelpharma →
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.