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CorTex SunX 50 Thick Avobenzone, Homosalate, Octisalate, Octocrylene 10 g/100mL; 5 g/100mL; 5 g/100mL; 3 g/100mL Lotion, 60 mL — NDC 65753-0603-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

CorTex SunX 50 Thick Avobenzone, Homosalate, Octisalate, Octocrylene 10 g/100mL; 5 g/100mL; 5 g/100mL; 3 g/100mL Lotion, 60 mL — NDC 65753-603-02 (Billing 65753-0603-02)

by CoreTex Products Inc · 60 mL in 1 BOTTLE, PLASTIC

This is a package of 60 mL of CorTex SunX 50 Thick Avobenzone, Homosalate, Octisalate, Octocrylene 10 g/100mL; 5 g/100mL; 5 g/100mL; 3 g/100mL Lotion from CoreTex Products Inc, no longer marketed (first marketed Mar 2023), no longer in the FDA NDC Directory.

NDC 65753-0603-02
🏷️ FDA NDC (as labeled) 65753-603-02 billing pads the product segment with a zero
This package
Contains60 mL Pack sizes19 compare ↓
Product page 65753-0603-01 Also comes in: 7 ml 65753-603-39 25 pouches 65753-603-22 25 pouches 65753-603-23 30 ml 65753-603-01 44 ml 65753-603-32 50 pouches 65753-603-24 60 ml 65753-603-33 100 pouches 65753-603-25 118 ml 65753-603-03 118 ml 65753-603-34 177 ml 65753-603-04 237 ml 65753-603-05 300 pouches 65753-603-26 473 ml 65753-603-07 762 ml 65753-603-08 762 ml 65753-603-35 946 ml 65753-603-09 3788 ml 65753-603-10
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Oct 2024. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65753-603-02
Product NDC 65753-603
11-digit billing NDC 65753060302
UNII G63QQF2NOX, 5A68WGF6WM, V06SV4M95S, 4X49Y0596W
UPC 0698229616722, 0698229616760, 0698229616678, 0698229616623 +9 more
Application # M020
SPL Set ID f67a6c6c-c314-1c9d-e053-2a95a90a7f1a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Oct 2024)
Marketing start 2023-03-09
Route TOPICAL
Dosage form LOTION
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
Why two NDCs? The FDA registers this code as 65753-603-02 — 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 → 65753-0603-02. 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?

CorTex SunX 50 is a topical lotion containing four UV-filtering ingredients: avobenzone, homosalate, octisalate, and octocrylene. These active ingredients are commonly used together in sunscreen products to absorb ultraviolet light and reduce sun exposure to the skin. This is an over-the-counter monograph drug, meaning it is marketed under FDA's established category rules for sunscreen products rather than as an individually approved 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.

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.
Try another pack size: 7 ml 25 pouches 25 pouches 30 ml 44 ml 50 pouches 60 ml 100 pouches 118 ml 118 ml 177 ml 237 ml 300 pouches 473 ml 762 ml 762 ml 946 ml 3788 ml
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
65753-0603-01 65753-603-01 Main listing 30 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-02 You're viewing this 60 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-03 65753-603-03 118 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-04 65753-603-04 177 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-05 65753-603-05 237 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-07 65753-603-07 473 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-09 65753-603-09 946 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-10 65753-603-10 3788 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-22 65753-603-22 25 POUCH in 1 CONTAINER / 7 mL in 1 POUCH 2023-01-03 — Discontinued by firm
65753-0603-23 65753-603-23 25 POUCH in 1 CONTAINER / 7 mL in 1 POUCH 2023-01-03 — Discontinued by firm
65753-0603-24 65753-603-24 50 POUCH in 1 CONTAINER / 7 mL in 1 POUCH 2023-01-03 — Discontinued by firm
65753-0603-25 65753-603-25 100 POUCH in 1 CONTAINER / 7 mL in 1 POUCH 2023-01-03 — Discontinued by firm
65753-0603-26 65753-603-26 300 POUCH in 1 CARTON / 7 mL in 1 POUCH 2023-01-03 — Discontinued by firm
65753-0603-32 65753-603-32 44 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-33 65753-603-33 60 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-34 65753-603-34 118 mL in 1 BOTTLE, PLASTIC 2023-01-03 — Discontinued by firm
65753-0603-39 65753-603-39 7 mL in 1 POUCH 2023-01-03 — Discontinued by firm
65753-0603-08 65753-603-08 762 mL in 1 BOTTLE, DISPENSING 2023-03-09 — Active
65753-0603-35 65753-603-35 762 mL in 1 BOTTLE 2023-03-09 — Active

Pack size FAQ

What quantity is in this package?
This package contains 60 mL — 60 ml in 1 bottle, plastic.
How does this package differ from NDC 65753-0603-39?
Both are CorTex SunX 50 Thick Avobenzone, Homosalate, Octisalate, Octocrylene 10 g/100mL; 5 g/100mL; 5 g/100mL; 3 g/100mL Lotion — the drug itself is identical. This page's package is the 60 mL one, while NDC 65753-0603-39 is the 7 ml package.
What NDC number is used to bill for this package of CorTex SunX 50 Thick Avobenzone, Homosalate, Octisalate, Octocrylene 10 g/100mL; 5 g/100mL; 5 g/100mL; 3 g/100mL Lotion?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
CorTex SunX 50 Thick 10 g/100mL; 5 g/100mL; 5 g/100mL; 3 g/100mLthis 65753-0603-02 CoreTex 60 ml — — Discontinued —
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

🏛️
2023
On the market since
Mar 2023
📍
2026
Currently FDA-listed
3 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.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 4GXD0Q3OS3
    A synthetic polymer made from acrylic compounds, crosslinked to form a network structure. It acts as a thickener, stabilizer, and suspending agent in liquid and gel formulations, helping maintain consistent texture and keep ingredients evenly distributed.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII Y15I6XI14C
    An oily liquid derived from petroleum, C12-20 alkyl benzoate serves as a solvent and emollient in medicines. It helps dissolve other ingredients and gives the product a smooth, spreadable texture.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII 6V475AX06U
    A chelating agent derived from ethylenediaminetetraacetic acid (EDTA) combined with copper. It binds metals in formulations to prevent discoloration and degradation, helping preserve the medicine's stability and appearance.
  • 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 3W404QE89S
    A plastic polymer made from ethylene that forms a flexible, durable solid. It's used as a coating or film-forming agent to protect the medicine and control how fast the active ingredient is released in the body.
  • UNII Z944H5SN0H
    A plant-based thickening agent derived from cellulose. It acts as a binder to hold tablet ingredients together and as a thickener in liquid formulations to achieve the right consistency.
  • UNII 58O7V09UCI
    A surfactant derived from sorbitol and oleic acid, used to help dissolve, mix, and stabilize oils and other hard-to-blend ingredients in liquid medicines and creams.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII EB048G1S9J
    A powder made from whole cacao beans, ground into a fine ingredient. Used as a flavor and filler to add taste and bulk to medicines, especially tablets and powders.
  • 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.

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

The official label also statesacrylates/C10-30 alkyl acrylate crosspolymer, aloe barbedensis leaf juice, C12-15 alkyl benzoate,carbomer, disodium EDTA, ethylhexylglycerin, hydroxypropyl methylcellulose, phenoxyethanol,polyethylene, polysorbate 20, propylene glycol, sodium hydroxide, sorbitan oleate, theobroma cacao (cocoa) seed butter, tocopheryl acetate, water.

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

LabelerCoreTex Products Inc
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code65753
First marketedMar 2023
Product typeHuman Otc Drug
Portfolio11 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.

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Patient Package Insert 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 27 words ▾

Uses: helps prevent sunburn. higher SPF gives more sunburn protection. retains SPF after 80 minutes of activity in the water or sweating. provides high protection against sunburn.

⏱️ Dosage and Administration 35 words ▾

Directions: apply liberally 15 minutes before sun exposure. Reapply: after 80 minutes of swimming or sweating after towel drying, swimming, or at least every 2 hours Children under 6 months of age: ask a doctor.

⚠️ Warnings 58 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 or irritation develops and lasts Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 6 words ▾

Active Ingredients: Avobenzone...3% Homosalate...10% Octisalate...5% Octocrylene...5%

🧪 Inactive Ingredients 35 words ▾

Inactive ingredients acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbedensis leaf juice, C12-15 alkyl benzoate,carbomer, disodium EDTA, ethylhexylglycerin, hydroxypropyl methylcellulose, phenoxyethanol,polyethylene, polysorbate 20, propylene glycol, sodium hydroxide, sorbitan oleate, theobroma cacao (cocoa) seed butter, tocopheryl acetate, water.

🎯 Purpose 5 words ▾

Purpose Sunscreen Sunscreen Sunscreen 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 13 words ▾

Stop use and ask a doctor if rash or irritation develops and lasts

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Other Information 38 words ▾

Other Information: Protect this product from excessive heat and direct sun. Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

📄 Questions or Comments 3 words ▾

Questions? Call: 1-877-684-5774

📄 Patient Package Insert 2 words ▾

65753-603-09 604-09

📄 Package Label / Principal Display Panel 31 words ▾

65753-602-24 602-24

65753-602-22,-23,-26,and -31 602

65753-603-03 604-03

65753-603-22,-23,-24,-25,-26 603-22

65753-603-10 604-10

65753-603-35 604-35

65753-603-02 604-02

65753-603-01 604-01

65753-603-33 604-33

65753-603-07 604-07

65753-603-05 604-05

65753-603-04 604-04

65753-603-34 604-34

65753-603-32 604-32

65753-603-39 603-39

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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 18 other package presentations of this same product, including 7 ml (65753-0603-39), 25 pouches (65753-0603-22), 25 pouches (65753-0603-23). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
CoreTex Products Inc 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.
← 65753-0602-22 · CoreTex 65753-0707-40 · CoreTex →
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.