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TriLipiderm Broad Spectrum SPF 30 Butyl Methoxydibenzoylmethane, Ethylhexyl methoxycinnamate, Homosalate, Octocrylene 3 g/100mL; 7.5 g/100mL; 10 g/100mL; 2.7 g/100mL Cream — NDC 60892-0601-05 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

TriLipiderm Broad Spectrum SPF 30 Butyl Methoxydibenzoylmethane, Ethylhexyl methoxycinnamate, Homosalate, Octocrylene 3 g/100mL; 7.5 g/100mL; 10 g/100mL; 2.7 g/100mL Cream — NDC 60892-601-05 (Billing 60892-0601-05)

by TriLipid Research Institute, LLC · 1 TUBE in 1 BOX / 89 mL in 1 TUBE

This is a package of TriLipiderm Broad Spectrum SPF 30 Butyl Methoxydibenzoylmethane, Ethylhexyl methoxycinnamate, Homosalate, Octocrylene 3 g/100mL; 7.5 g/100mL; 10 g/100mL; 2.7 g/100mL Cream from TriLipid Research Institute, LLC, marketed since Jan 2014 and currently FDA-listed.

NDC 60892-0601-05
🏷️ FDA NDC (as labeled) 60892-601-05 billing pads the product segment with a zero
This package
Contains89 mL in 1 tube Pack sizes7 compare ↓
Product page 60892-0601-00 Also comes in: 237 mL 60892-601-04 4 ml 60892-601-77 9 ml 60892-601-00 29.625 ml 60892-601-01 948 ml 60892-601-32 1896 ml 60892-601-64
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 60892-601-05 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
60892 labeler · 601 product · 05 package
Package marketed since
Dec 13, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0855269007488
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 60892-601-05
Product NDC 60892-601
11-digit billing NDC 60892060105
UNII G63QQF2NOX, 4Y5P7MUD51, V06SV4M95S, 5A68WGF6WM
UPC 0855269007488
Application # M020
SPL Set ID 617fc696-c2a1-4855-bafb-0454e6497101
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-01-31
Route TOPICAL
Dosage form CREAM
Substance AVOBENZONE; OCTINOXATE; HOMOSALATE; OCTOCRYLENE
Why two NDCs? The FDA registers this code as 60892-601-05 — 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 → 60892-0601-05. 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?

TriLipiderm Broad Spectrum SPF 30 is a topical cream containing four active ingredients that function as ultraviolet (UV) filters. Avobenzone, homosalate, octinoxate, and octocrylene are commonly used together in sunscreen products to help absorb and scatter UVA and UVB radiation from the sun. This is an over-the-counter monograph drug, meaning it is marketed under the FDA's established rules for sunscreen products rather than through an individual product 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: 237 mL 4 ml 9 ml 29.625 ml 948 ml 1896 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
60892-0601-00 60892-601-00 Main listing 9 mL in 1 PACKET 2014-01-31 — Active
60892-0601-01 60892-601-01 29.625 mL in 1 TUBE 2014-01-31 — Active
60892-0601-04 60892-601-04 1 BOTTLE, PUMP in 1 BOX / 237 mL in 1 BOTTLE, PUMP 2014-01-31 — Active
60892-0601-05 You're viewing this 1 TUBE in 1 BOX / 89 mL in 1 TUBE 2018-12-13 — Active
60892-0601-32 60892-601-32 948 mL in 1 BOTTLE, PUMP 2014-01-31 — Active
60892-0601-64 60892-601-64 1896 mL in 1 BOTTLE, PUMP 2014-01-31 — Active
60892-0601-77 60892-601-77 4 mL in 1 PACKET Sample 2018-12-12 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 tube in 1 box / 89 ml in 1 tube.
What NDC number is used to bill for this package of TriLipiderm Broad Spectrum SPF 30 Butyl Methoxydibenzoylmethane, Ethylhexyl methoxycinnamate, Homosalate, Octocrylene 3 g/100mL; 7.5 g/100mL; 10 g/100mL; 2.7 g/100mL Cream?
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
TriLipiderm Broad Spectrum SPF 30 3 g/100mL; 7.5 g/100mL; 10 g/100mL; 2.7 g/100mLthis 60892-0601-05 TriLipid 1 tube — — 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

🏛️
2014
On the market since
Jan 2014
📍
2026
Currently FDA-listed
12 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 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • 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 18E7415PXQ
    A plant extract from calendula flowers used in topical formulations. It functions as a soothing botanical ingredient and may help support the product's skin-conditioning properties.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 1C6V77QF41
    Cholecalciferol is vitamin D3, a fat-soluble vitamin added to medicines as a nutritional supplement or active ingredient fortification. It helps the body absorb calcium and support bone health.
  • UNII 3885PD1IZ8
    A plant-derived ingredient from the Abyssinian crambe plant. It functions as a natural binder or filler to help hold the medicine's components together and give the tablet or capsule its shape and structure.
  • UNII 11A386X1QH
    Dodecane is a clear, colorless liquid hydrocarbon derived from petroleum. It functions as a solvent and lubricant in medicines, helping dissolve active ingredients and improve how the product flows during manufacturing.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • UNII 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII DKY81513ER
    Limnanthes alba whole is a plant-derived ingredient, commonly known as meadowfoam seed. It's used in formulations as an emollient and conditioning agent to help soften and smooth the product's texture.
  • UNII 6M3P64V0NC
    A fine powder made from magnesium, aluminum, and silicon compounds. It absorbs moisture and helps keep medicine ingredients from clumping or separating, so the product stays stable and flows smoothly during manufacturing.
  • UNII 3HH93SL2H9
    A plant-derived oil made from meadowfoam seeds. It acts as an emollient and lubricant in medicines, helping soften formulations and improve how ingredients mix together.
  • UNII XO45V955LT
    A natural oil extract from olives that contains compounds resistant to saponification. Used as an emollient and skin-conditioning agent to improve product texture and spreadability in topical formulations.
  • 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 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 YRC528SWUY
    A waxy emulsifier made from plant-derived fatty alcohols. It helps blend oil and water-based ingredients together and improves how the medicine spreads and absorbs.
  • 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 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 65UEH262IS
    Safflower oil is a plant-based oil extracted from safflower seeds. It's used in medicines as a solvent and carrier to help dissolve or suspend active ingredients, and sometimes as an emollient to improve texture.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • 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 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • 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.

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

The official label also statesAcrylates/C10-30 Alkyl Acrylate Crosspolymer, Aqua (Deionized Water), Butylene Glycol, Calendula Officinalis Extract, Carthamus Tinctorius (Safflower) Oil, Caprylyl Glycol, Ceteareth-20, Chamomilla Matricaria (Chamomile) Extract, Cholecalciferol (Vitamin B3), Crambe Abyssinica (Abyssinian) Oil, Dodecane, Gluconolactone, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Helianthus Annuus (Sunflower) Wax, Hexylene Glycol, Limnanthes Alba (Meadowfoam) Oil, Magnesium Aluminum Silicate, Meadowfoam Estolide, o-Cymen-5-ol, Olea Europeaea (Olive) Fruit Unsaponifiables, dl-Panthenol, Partum (Fragrance), Phenoxyethanol, Phytosterols, Polysorbate 20, Potassium Sorbate, Simmondsia Chinensis (Jojoba) Oil, Tocopherol (Vitamin E), Triethanolamine, Xanthan Gum.

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

LabelerTriLipid Research Institute, LLC
FDA applicationM020 (OTC MONOGRAPH DRUG)
Labeler code60892
First marketedJan 2014
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from TriLipid Research Institute, LLC labeler code 60892

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 29 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

⏱️ Dosage and Administration 93 words ▾

Directions: Apply liberally 15 minutes before sun exposure Use a water resistant sunscreen if swimming or sweating Reapply at least every 2 hours Children under 6 months: ask a doctor 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 10:00 AM – 2:00 PM Wear long sleeved shirts, pants, hats, and sunglasses

⚠️ Warnings 5 words ▾

Warnings For External Use Only

📦 Storage and Handling 11 words ▾

Other Information Protect this product from excessive heat and direct sun

🧪 Active Ingredient 12 words ▾

Active Ingredients Butyl Methoxydibenzoylmethane 3%, Ethylhexyl Methoxycinnamate 7.5%, Homosalate 10%, Octocrylene 2.7%

🧪 Inactive Ingredients 80 words ▾

Inactive Ingredients: Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aqua (Deionized Water), Butylene Glycol, Calendula Officinalis Extract, Carthamus Tinctorius (Safflower) Oil, Caprylyl Glycol, Ceteareth-20, Chamomilla Matricaria (Chamomile) Extract, Cholecalciferol (Vitamin B3), Crambe Abyssinica (Abyssinian) Oil, Dodecane, Gluconolactone, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Helianthus Annuus (Sunflower) Wax, Hexylene Glycol, Limnanthes Alba (Meadowfoam) Oil, Magnesium Aluminum Silicate, Meadowfoam Estolide, o-Cymen-5-ol, Olea Europeaea (Olive) Fruit Unsaponifiables, dl-Panthenol, Partum (Fragrance), Phenoxyethanol, Phytosterols, Polysorbate 20, Potassium Sorbate, Simmondsia Chinensis (Jojoba) Oil, Tocopherol (Vitamin E), Triethanolamine, Xanthan Gum.

🎯 Purpose 2 words ▾

Purpose 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 9 words ▾

Stop Use and Ask a Doctor If Rash Occurs

📄 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

📄 Package Label / Principal Display Panel 10 words ▾

All-Body Moisture Retention Creme Broad Spectrum SPF 30 Sample Image

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
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 TriLipid Research Institute, LLC. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 6 other package presentations of this same product, including 1 bottle (60892-0601-04), 4 ml (60892-0601-77), 9 ml (60892-0601-00). 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?
TriLipid Research Institute, 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.
← 60885-0040-00 · FAREVA 60892-0602-16 · TriLipid →
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.