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Clinical Skin Filter Tinted Sunscreen Medium Dark 1.182 mg/30mL; 1.734 mg/30mL; .9 mg/30mL Cream, 30 mL

by KRX RESOURCES SDN. BHD. · 30 mL in 1 PACKAGE (84755-0004-1)
NDC 84755-0004-01
🏷️ FDA NDC (as labeled) 84755-0004-1 billing pads the package segment with a zero
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) 84755-0004-1
Product NDC 84755-0004
11-digit billing NDC 84755000401
UNII SOI2LOH54Z, 15FIX9V2JP, 5A68WGF6WM
SPL Set ID 22cead37-f862-e859-e063-6394a90a86ce
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-09-01
Route TOPICAL
Dosage form CREAM
Substance ZINC OXIDE; TITANIUM DIOXIDE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 84755-0004-1 — a 5-4-1 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 package segment → 84755-0004-01. 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

LabelerKRX RESOURCES SDN. BHD.
Labeler code84755
First marketedSep 2024
Product typeHuman Otc Drug
Portfolio7 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 is a tinted sunscreen cream applied to the skin. It contains three active ingredients: octocrylene, titanium dioxide, and zinc oxide. Titanium dioxide and zinc oxide are mineral UV filters that work by reflecting and scattering ultraviolet light away from the skin. Octocrylene is an organic UV filter that absorbs ultraviolet rays. Together, these ingredients are typically used in sunscreen products intended to provide sun protection and reduce UV exposure 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.

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

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • 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 V2W71V8T0X
    A silicone-based compound that mixes oil and water together. Used in formulations as an emulsifier to help blend ingredients and improve texture and stability of creams, lotions, and other topical products.
  • UNII 98TEA9T639
    Crataegus cuneata fruit is a plant extract from hawthorn berries. It may be used as a filler or binding agent to add bulk and help hold tablet or capsule ingredients together.
  • UNII RO266O364U
    Dimethicone is a silicone-based lubricant and anti-foaming agent. It reduces friction between particles and prevents foam formation in liquid or semi-solid medicines, helping with smooth mixing and texture.
  • UNII X687XDK09L
    A clay mineral processed to carry positive charges, used as a thickener and suspending agent in liquid medicines. It helps keep solid particles evenly distributed throughout the product.
  • UNII S3KFG6Q5X8
    An organic chemical compound used as a UV filter in topical formulations. It helps protect the medicine or product from degradation caused by sunlight exposure during storage and use.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII ZP9XFG71A7
    A plant extract from ivy leaves used as a natural ingredient. It may function as a preservative, emollient, or flavoring agent in medications and topical formulations.
  • UNII 113171Q70B
    Lauroyl lysine is a compound made by combining an amino acid (lysine) with a fatty acid (lauric acid). It works as a glidant and lubricant to help powder particles flow smoothly during manufacturing and tablet compression.
  • UNII NDT563S5VZ
    A salt derived from the chemical compound EDTA, used as a chelating agent and preservative. It binds to metal ions in the formulation to prevent spoilage and maintain product stability.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII XOF597Q3KY
    A refined form of wax made from petroleum, microcrystalline wax is used in medicines as a coating agent, binder, and hardening ingredient. It helps give tablets and capsules their shape and protective outer layer.
  • UNII 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII 9713Q0S7FO
    A synthetic emulsifier derived from polyethylene glycol and fatty acids. It helps blend water and oil-based ingredients together in the formulation, improving texture and stability.
  • UNII K29QC5YCW8
    Pentamethyl cyclopentasiloxane is a silicone-based liquid used in medications as a skin-conditioning agent and lubricant. It helps the product spread smoothly and reduces friction on skin or in the mouth.
  • UNII YI4N487572
    A mineral salt combination containing potassium, magnesium, and sulfate. It may be used in formulations as a buffer to help maintain pH balance or as a filler to add bulk to the medicine.
  • UNII U08429QT99
    A plant extract from peach fruit and plant material used in some formulations as a flavoring agent or natural ingredient to add taste and aroma to the medicine.
  • UNII 80UKV9Y4B3
    A plant extract from common pear fruit used as a natural flavoring agent and sweetener in medicines. It adds taste appeal and may help mask bitter drug flavors in oral formulations.
  • UNII O7757NO1VL
    A synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in liquid formulations. It helps extend the shelf life of medicines by inhibiting microbial contamination.
  • UNII MDL271E3GR
    Sorbitan olivate is an emulsifier derived from sorbitol and olive oil. It helps blend water and oil ingredients together to maintain consistent texture and appearance throughout the medicine.
  • UNII 0W8RRI5W5A
    A fatty acid derivative used as an emulsifier and surfactant in medications. It helps blend oily and water-based ingredients together to create a stable, uniform product.
  • UNII LDC331P08E
    A silicone-based compound that acts as a glidant and flow agent in solid medications. It reduces friction between powder particles, helping the medicine flow smoothly during manufacturing and tablet compression.
  • UNII BOS0R5Y21O
    A flavoring ingredient derived from vanilla orchid pods. It adds vanilla taste and aroma to make the medicine more palatable, especially in products for children or those requiring better taste masking.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesInactive Ingredients: Water, Cyclopentasiloxane, Ethylhexyl Methoxycinnamate, Titanium Dioxide, Ethylhexyl Salicylate, Zinc Oxide, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Octocrylene, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, Methylpropanediol, Niacinamide, 1,2- Hexanediol, Dimethicone, Disteardimonium Hectorite, Sorbitan Olivate, Sorbitan Sesquioleate, Microcrystalline Wax, Lauroyl Lysine, Magnesium Sulfate, PEG-30 Dipolyhydroxystearate, Quaternium-18 Bentonite, CI 77492, Silica, Triethoxycaprylylsilane, CI 77491, Crataegus Cuneata Fruit Extract, Prunus Persica (Peach) Fruit Extract, Pyrus Communis (Pear) Fruit Extract, Ethylhexylglycerin, CI 77499, Adenosine, Hedera Helix (Ivy) Extract, Vanilla Planifolia Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Disodium EDTA, BHT, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate.

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 gPer 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
Clinical Skin Filter Tinted Sunscreen Medium Dark 1.182 mg/30mL; 1.734 mg/30mL; .9 mg/30mLthis 84755-0004-01 KRX 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
Sep 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
84755-0004-01 You're viewing this 30 mL in 1 PACKAGE (84755-0004-1) 2024-09-01 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 "Unapproved Drug Other". 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 84755-0004-1, 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: 84755-0004-01, written without dashes as 84755000401. 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 84755-0004-01, the first segment (84755) is the labeler code FDA assigned to KRX RESOURCES SDN. BHD.; the middle segment (0004) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 KRX RESOURCES SDN. BHD.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
KRX RESOURCES SDN. BHD. 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 90 words ▾

Our CLINICAL SKIN FILTER Mineral Tinted Sunscreen does not leave a white cast, dries on matte, blurs the pores and just leaves skin smooth and photo ready! The tint blends in, and It feels like a second skin, It is also water resistant, and helps skin recover from existing sun damage. It can be used under make up without leaving clumped and patchy areas.

This product is really like no other, and you will love every application. -Pore Blurring -Ultra Matte -Non Comedogenic -White Cast cancellation -Picture perfect CRUELTY FREE.

⏱️ Dosage and Administration 23 words ▾

Use fingertips and apply all over face and neck, Apply liberally before sun exposure and reapply after 60 minutes of swimming and/or sweating.

⚠️ Warnings 51 words ▾

Warning: Spending time under the sun for long period time increases your risk of skin cancer and early signs of ageing. External Use Only. If Irritation occurs, stop using and consult your doctor. Keep out of reach of children. If product is swallowed, get medical help or contact poison control immediately.

🧪 Active Ingredient 13 words ▾

Active: Cyclopentasiloxane -8% Titanium Dioxide - 5.78% Zinc Oxide - 3.94% Octocrylene -3%

🧪 Inactive Ingredients 85 words ▾

Inactive Ingredients: Water, Cyclopentasiloxane, Ethylhexyl Methoxycinnamate, Titanium Dioxide, Ethylhexyl Salicylate, Zinc Oxide, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Octocrylene, Cetyl PEG/PPG-10/1 Dimethicone, Glycerin, Methylpropanediol, Niacinamide, 1,2- Hexanediol, Dimethicone, Disteardimonium Hectorite, Sorbitan Olivate, Sorbitan Sesquioleate, Microcrystalline Wax, Lauroyl Lysine, Magnesium Sulfate, PEG-30 Dipolyhydroxystearate, Quaternium-18 Bentonite, CI 77492, Silica, Triethoxycaprylylsilane, CI 77491, Crataegus Cuneata Fruit Extract, Prunus Persica (Peach) Fruit Extract, Pyrus Communis (Pear) Fruit Extract, Ethylhexylglycerin, CI 77499, Adenosine, Hedera Helix (Ivy) Extract, Vanilla Planifolia Fruit Extract, Musa Sapientum (Banana) Fruit Extract, Disodium EDTA, BHT, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate.

🎯 Purpose 42 words ▾

FOR ALL SKIN TYPES WATER & SWEAT RESISTANT (60 MINUTES) CLINICAL SKIN FILTER Mineral Tinted Sunscreen TRANSLUCENT Light/Medium Directions: Use fingertips and apply all over face and neck, Apply liberally before sun exposure and reapply after 60 minutes of swimming and/or sweating.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84755-0003-01 · KRX 84755-0005-01 · KRX →
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.