Home › NDC Lookup › Ingredients › Transparent Gel Sunscreen Spf50 › 85885-0121-01
Transparent Gel Sunscreen SPF50, Flirt with the Sun 3 g/100mL; 7 g/100mL; 5 g/100mL; 9 g/100mL Cream, 50 mL — NDC 85885-0121-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Transparent Gel Sunscreen SPF50, Flirt with the Sun 3 g/100mL; 7 g/100mL; 5 g/100mL; 9 g/100mL Cream, 50 mL — NDC 85885-121-01 (Billing 85885-0121-01)

by Latin Beauty LLC · 50 mL in 1 BOTTLE

This is a package of 50 mL of Transparent Gel Sunscreen SPF50, Flirt with the Sun 3 g/100mL; 7 g/100mL; 5 g/100mL; 9 g/100mL Cream from Latin Beauty LLC, no longer marketed (first marketed Jul 2025), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 85885-0121-01
🏷️ FDA NDC (as labeled) 85885-121-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 85885-121-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85885 labeler · 121 product · 01 package
Package marketed since
Jul 11, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8588512101 0
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. 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) 85885-121-01
Product NDC 85885-121
11-digit billing NDC 85885012101
UNII 4X49Y0596W, V06SV4M95S, 5A68WGF6WM, G63QQF2NOX
Application # M016
SPL Set ID 3a234cf5-ee7c-8dcf-e063-6294a90a629c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2025-07-11
Route TOPICAL
Dosage form CREAM
Substance OCTISALATE; HOMOSALATE; OCTOCRYLENE; AVOBENZONE
Why two NDCs? The FDA registers this code as 85885-121-01 — 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 → 85885-0121-01. 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.

Clinical

🧪 What is this product?

This is a topical sunscreen cream containing four UV-filtering agents: avobenzone, homosalate, octisalate, and octocrylene. These active ingredients are typically used together to absorb and scatter ultraviolet light from the sun, helping to reduce skin exposure to UV radiation. The product is marketed as an over-the-counter monograph sunscreen, meaning it follows FDA's established safety and effectiveness rules for this product category rather than being individually reviewed.

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.
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
85885-0121-01 You're viewing this Main listing 50 mL in 1 BOTTLE 2025-07-11 — Inactivated by FDA

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Transparent Gel Sunscreen SPF50, Flirt with the Sun 3 g/100mL; 7 g/100mL; 5 g/100mL; 9 g/100mLthis 85885-0121-01 Latin 50 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

🏛️
2025
On the market since
Jul 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.

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 O4I3UFO6ZF
    A silicone-based polymer blend that acts as an emulsifier and texture modifier. It helps keep oil and water mixed together in the formulation and gives the product a smooth, spreadable consistency.
  • UNII 9E4CO0W6C5
    A silicone-based polymer that forms soft, spongy particles. Used as a texture modifier and suspending agent to improve how the product feels and flows, and to help keep ingredients evenly distributed throughout the formulation.
  • UNII A8289P68Y2
    Isododecane is a lightweight liquid hydrocarbon used as a solvent and spreadability agent in topical formulations. It helps dissolve active ingredients and makes the product easier to apply and absorb into the skin.
  • UNII 918X1OUF1E
    Isohexadecane is a synthetic hydrocarbon oil used as an emollient and solvent in topical medicines. It helps dissolve active ingredients and improves spreadability and absorption through the skin.
  • 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.

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

The official label also statesIsohexadecane, Dimethicone/Vinyl DimethiconeCrosspolymer, lsododecane, Dimethicone/Bis-sobutyPpg20 Crosspolymer, 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.

Manufacturer & labeler

LabelerLatin Beauty LLC
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code85885
First marketedJul 2025
Product typeHuman Otc Drug
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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 82 words ▾

Directions Apply liberally 15 minutes before sun exposure..Reapply: at least every 2 hours. After 40 or 80 minutesof swimming or sweating.lmmediately after toweldrying..Sun Protection Measures: Spending time in the sunincreases your risk of skin cancer and early skin agingTo decrease this risk, regularly use a sunscreen with aBroad Spectrum SPF of 15 or higher and othEr sunprotection measures including: limit time in sun,especially from 10 a.m.-2 p.m., and wear long-sleevedshirts, pants, hats and sunglasses. Children under 6months of age: ask a doctor.

⏱️ Dosage and Administration 23 words ▾

Apply liberally 15 minutes before sun exposure.Reapply: at least every 2 hours. After 40 or 80 minutesof swimming or sweating. lmmediately after toweldrying.

⚠️ Warnings 81 words ▾

WarningsFor extemal use only, Do not use on damaged or broken skin.When using this product: keep out of eyes. Rinse withwater to remove.Stop use and ask a doctor if rash occurs.Keep out of reach of children. lf swallowed, get medicalhelp or contact a Poison Control Center right away. UVexposure from the sun increases the risk of skin cancer,premature skin aging, and other skin damage. lt isimportant to decrease UV exposure by limiting time inthe sun, wearing protective clothing, and using asunscreen.

🧪 Active Ingredient 6 words ▾

ACTIVE INGRENDIENT Octocrylene Homosalate Octisalate Avobenzone

🧪 Inactive Ingredients 7 words ▾

Isohexadecane, Dimethicone/Vinyl DimethiconeCrosspolymer, lsododecane, Dimethicone/Bis-sobutyPpg20 Crosspolymer, Tocopherol

🎯 Purpose 1 words ▾

Sunscreen

📄 When Using This Product 26 words ▾

Uses Helps prevent sunburn.If used as directed with other sun protection measures(see Directions), decreases the risk of skin cancer andearly skin aging caused by the sun.

📄 Stop Use and Ask a Doctor If 59 words ▾

Stop use and ask a doctor if rash occurs.Keep out of reach of children. lf swallowed, get medicalhelp or contact a Poison Control Center right away. UVexposure from the sun increases the risk of skin cancerpremature skin aging, and other skin damage. lt isimportant to decrease UV exposure by limiting time inthe sun, wearing protective clothing, and using asunscreen.

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children. lf swallowed, get medicalhelp or contact a Poison Control Center right away.

📄 Other Information 13 words ▾

Other information Protect this product in this container from excessiveheat and direct sun.

📄 Package Label / Principal Display Panel 1 words ▾

labeling

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.
Who lists this product with the FDA?
Latin Beauty 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.
← 85884-0261-04 · Steel 85886-0202-50 · FRANCISCO →
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.