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Pfect A solar barrier Serum Textured 1.5 mg/50mL; 2.5 mg/50mL Elixir, 50 mL — NDC 84755-0002-01 package photo

Pfect A solar barrier Serum Textured 1.5 mg/50mL; 2.5 mg/50mL Elixir, 50 mL

by KRX RESOURCES SDN. BHD. · 50 mL in 1 PACKAGE (84755-0002-1)
NDC 84755-0002-01
🏷️ FDA NDC (as labeled) 84755-0002-1 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) 84755-0002-1
Product NDC 84755-0002
11-digit billing NDC 84755000201
UNII XQN8R9SAK4, ANQ870JD20
SPL Set ID 22b75c05-1391-a00c-e063-6394a90aa7ad
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 ELIXIR
Substance ETHYLHEXYL TRIAZONE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE
Why two NDCs? The FDA registers this code as 84755-0002-1 — 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 → 84755-0002-01. 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?

Pfect A Solar Barrier Serum Textured is a topical elixir containing two active ingredients, diethylamino hydroxybenzoyl hexyl benzoate and ethylhexyl triazone, which are ultraviolet (UV) light absorbers commonly found in sunscreen products. These ingredients are typically used to help protect skin from UV radiation when applied to the skin. This product is marketed without an approved FDA application.

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 L4EL31FWIL
    A synthetic peptide (short chain of amino acids) used as a conditioning or texture-enhancing agent in topical formulations. It helps improve product feel and skin compatibility in creams and lotions.
  • UNII K72T3FS567
    Adenosine is a naturally occurring nucleoside compound. In medicines, it functions as an active pharmaceutical ingredient in some formulations, though when listed as an excipient it may serve as a buffering or stabilizing agent to maintain product stability and pH.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII Z135WT9208
    Carbomer is a synthetic polymer that forms a thick, gel-like consistency. It's used in medicines as a thickener and stabilizer to improve texture and keep ingredients evenly mixed throughout the product.
  • UNII 4Q93RCW27E
    A synthetic polymer made from acrylic acid that's crosslinked for stability. It acts as a thickener and gelling agent in creams and gels, helping the medicine spread evenly and maintain its texture.
  • UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • UNII 7RXW88PS4S
    A synthetic oily liquid derived from caprylic and capric acids. It serves as an emollient and solvent in topical formulations, helping active ingredients dissolve and spread smoothly on skin.
  • 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 GAN16C9B8O
    Glutathione is a naturally occurring antioxidant compound made from three amino acids. In medications, it may serve as an antioxidant to protect the drug's active ingredients from breaking down or degrading over time.
  • 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 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 WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 788QAG3W8A
    A synthetic polymer that combines polyethylene glycol, glycidyl ether, and sodium hyaluronate. It acts as a thickener and film-former in topical products, helping maintain texture and improve how the medicine spreads on skin.
  • UNII 50C1307PZG
    Pentylene glycol is a humectant and preservative helper derived from petroleum or plant sources. It draws moisture into the product and helps prevent bacterial growth, keeping medicines stable during storage.
  • UNII W19EIO0DBE
    A plant-derived emulsifier made from glycerin and fatty acids. It helps mix oil and water-based ingredients together and stabilizes the product's texture in creams, lotions, and other cosmetic or topical formulations.
  • UNII 59Z907ZB69
    A synthetic silicone polymer used as a glidant and anti-caking agent. It reduces friction between particles, helping powders and tablets flow smoothly during manufacturing and use.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • UNII 8LLD82AE3S
    A naturally derived sweetener and prebiotic carbohydrate extracted from sugar cane stems. It sweetens the medicine, improves taste, and may help with texture and stability in the formulation.
  • UNII 65A9F4P024
    A synthetic compound derived from the amino acid glutamate and stearic acid. It acts as an emulsifier and surfactant to help mix oil and water-based ingredients, keeping the medicine uniform throughout.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • UNII 023C2WHX2V
    Tromethamine is a chemical buffer that helps maintain the proper acidity level in liquid medicines. It neutralizes acids and stabilizes the solution so the medication remains effective and safe throughout its shelf life.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesInactive Ingredients: WATER, PROPANEDIOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, POLYMETHYLSILSESQUIOXANE, ETHYLHEXYL TRIAZONE, NIACINAMIDE, METHYLENE BIS- BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL, COCO- CAPRYLATE/CAPRATE, CAPRYLYL METHICONE, DIETHYLHEXYL BUTAMIDO TRIAZONE, GLYCERIN, SODIUM HYALURONATE, BUTYLENE GLYCOL, CAMELLIA SINENSIS LEAF EXTRACT, SACCHARUM OFFICINARUM (SUGARCANE) EXTRACT, ACETYL HEXAPEPTIDE-8, MACROCYSTIS PYRIFERA (KELP) EXTRACT, COCOS NUCIFERA (COCONUT) FRUIT EXTRACT, PANAX GINSENG ROOT EXTRACT, PANTHENOL, PENTYLENE GLYCOL, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, DECYL GLUCOSIDE, TROMETHAMINE, CARBOMER, 1,2- HEXANEDIOL,SODIUM STEAROYL GLUTAMATE, POLYACRYLATE CROSSPOLYMER-6, CARBOMER, ETHYLHEXYLGLYCERIN, ADENOSINE, XANTHAN GUM, GLUTATHIONE, TOCOPHEROL.

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Pfect A solar barrier Serum Textured 1.5 mg/50mL; 2.5 mg/50mL 87565-0002-01 BY 50 ml — — FDA listed —
Pfect A solar barrier Serum Textured 1.5 mg/50mL; 2.5 mg/50mLthis 84755-0002-01 KRX 50 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
84755-0002-01 You're viewing this 50 mL in 1 PACKAGE (84755-0002-1) 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 ✓ 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 "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 84755-0002-1, 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: 84755-0002-01, written without dashes as 84755000201. 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 84755-0002-01, the first segment (84755) is the labeler code FDA assigned to KRX RESOURCES SDN. BHD.; the middle segment (0002) 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 36 words ▾

Non Sticky and No white cast SPF 50 PA ++++ Suncreen formula, with UVA and UVB protection. Rich in Vitamins, Peptides and Nutrients for both hydration, anti ageing and sun protection. Suitable for all skin types.

⏱️ Dosage and Administration 11 words ▾

Directions: Apply liberally and spread evenly by hand before sun exposure.

⚠️ Warnings 28 words ▾

Warning: For External use only. Do not apply on damaged or broken skin. Keep out of reach of children. If irrational occurs, stop use and consult your doctor.

🧪 Active Ingredient 8 words ▾

Active: HYDROXYBENZOYL HEXYL BENZOATE 5% ETHYLHEXYL TRIAZONE 3%

🧪 Inactive Ingredients 74 words ▾

Inactive Ingredients: WATER, PROPANEDIOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, POLYMETHYLSILSESQUIOXANE, ETHYLHEXYL TRIAZONE, NIACINAMIDE, METHYLENE BIS- BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL, COCO- CAPRYLATE/CAPRATE, CAPRYLYL METHICONE, DIETHYLHEXYL BUTAMIDO TRIAZONE, GLYCERIN, SODIUM HYALURONATE, BUTYLENE GLYCOL, CAMELLIA SINENSIS LEAF EXTRACT, SACCHARUM OFFICINARUM (SUGARCANE) EXTRACT, ACETYL HEXAPEPTIDE-8, MACROCYSTIS PYRIFERA (KELP) EXTRACT, COCOS NUCIFERA (COCONUT) FRUIT EXTRACT, PANAX GINSENG ROOT EXTRACT, PANTHENOL, PENTYLENE GLYCOL, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, DECYL GLUCOSIDE, TROMETHAMINE, CARBOMER, 1,2- HEXANEDIOL,SODIUM STEAROYL GLUTAMATE, POLYACRYLATE CROSSPOLYMER-6, CARBOMER, ETHYLHEXYLGLYCERIN, ADENOSINE, XANTHAN GUM, GLUTATHIONE, TOCOPHEROL.

🎯 Purpose 52 words ▾

•Nourishing •Anti Ageing •Sun Protection Non Sticky and No white cast SPF 50 PA ++++ Suncreen formula, with UVA and UVB protection. Rich in Vitamins, Peptides and Nutrients for both hydration, anti ageing and sun protection. Suitable for all skin types. Directions: Apply liberally and spread evenly by hand before sun exposure.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 84755-0001-01 · KRX 84755-0003-01 · 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.