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Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mg Film, Soluble — NDC 84778-0089-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mg Film, Soluble — NDC 84778-089-02 (Billing 84778-0089-02)

by Guangzhou Yixin Cross-border E-commerce Co., Ltd. · 2 PATCH in 1 BOX / 40 mg in 1 PATCH

This is a package of Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mg Film, Soluble from Guangzhou Yixin Cross-border E-commerce Co., Ltd., no longer marketed (first marketed Aug 2025), no longer in the FDA NDC Directory.

NDC 84778-0089-02
🏷️ FDA NDC (as labeled) 84778-089-02 billing pads the product segment with a zero
This package
Contains40 mg in 1 patch Pack sizes4 compare ↓
Product page 84778-0089-01 Also comes in: 40 mg 84778-089-01 4 patches 84778-089-03 8 patches 84778-089-04
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 2, 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 84778-089-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84778 labeler · 089 product · 02 package
Package marketed since
Aug 24, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8477808902 4
FDA record last changed
Jul 2, 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) 84778-089-02
Product NDC 84778-089
11-digit billing NDC 84778008902
UNII 742SXX0ICT, UCE6F4125H
Application # 505G(a)(3)
SPL Set ID 3f3d7a07-51d5-fcca-e063-6294a90a4ba4
Established class (EPC) Phosphodiesterase 5 Inhibitor
Mechanism of action Phosphodiesterase 5 Inhibitors
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2025-08-24
Route TOPICAL
Dosage form FILM, SOLUBLE
Substance TADALAFIL; VARDENAFIL
Why two NDCs? The FDA registers this code as 84778-089-02 — 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 → 84778-0089-02. 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?

Esokalli Testosterone Booster is an over-the-counter oral dissolving film containing tadalafil and vardenafil. Both active ingredients are phosphodiesterase 5 inhibitors, a class of compounds typically used to address erectile dysfunction. This product is marketed as an OTC monograph drug, meaning it is sold under FDA's established rules for this category rather than through individual product approval. The film dissolves in the mouth for oral absorption.

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 eachPer 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: 40 mg 4 patches 8 patches
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
84778-0089-01 84778-089-01 Main listing 1 PATCH in 1 BOX / 40 mg in 1 PATCH 2025-08-24 — Inactivated by FDA
84778-0089-02 You're viewing this 2 PATCH in 1 BOX / 40 mg in 1 PATCH 2025-08-24 — Inactivated by FDA
84778-0089-03 84778-089-03 4 PATCH in 1 BOX / 40 mg in 1 PATCH 2025-08-24 — Inactivated by FDA
84778-0089-04 84778-089-04 8 PATCH in 1 BOX / 40 mg in 1 PATCH 2025-08-24 — Inactivated by FDA

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 2 patch in 1 box / 40 mg in 1 patch.
What NDC number is used to bill for this package of Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mg Film, Soluble?
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
Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mg 84778-0092-01 Guangzhou 1 patch — — Discontinued —
Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mgthis 84778-0089-02 Guangzhou 2 patches — — Discontinued —
Esokalli Testosterone Booster Oral Dissolving Film 30 mg/100mg; 10 mg/100mg 84778-0083-01 Guangzhou 1 patch — — 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
Aug 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 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • UNII 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
  • UNII C151H8M554
    A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.

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

The official label also statesFilm-forming polymers, stabilizers, sweeteners, flavoring agents.

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

LabelerGuangzhou Yixin Cross-border E-commerce Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code84778
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio29 products on file

More NDCs from Guangzhou Yixin Cross-border E-commerce Co., Ltd... labeler code 84778

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 🧪 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 8 words ▾

Uses For the treatment of erectile dysfunction (ED)

⏱️ Dosage and Administration 43 words ▾

Dosage and administration • Take 1 oral film as a single dose. • Administer orally by placing on the tongue until dissolved. • Administer approximately 0.5 to 4 hours prior to anticipated sexual activity. • Do not exceed 1 dose in 24 hours.

⚠️ Warnings 5 words ▾

Warnings For adult men only.

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients Film-forming polymers, stabilizers, sweeteners, flavoring agents.

🎯 Purpose 6 words ▾

Purpose Phosphodiesterase type 5 (PDE5) inhibitors

📄 Do Not Use 40 words ▾

Do not use if you: take nitrate medicines (such as nitroglycerin) have severe heart disease or very low blood pressure are allergic to tadalafil, vardenafil, or any ingredient in this product have galactose intolerance, total lactase deficiency, or glucose-galactose malabsorption

📄 When Using This Product 22 words ▾

When using this product you may experience: headache, flushing, indigestion, nasal congestion, dizziness, muscle pain, back pain, nausea, rash, or visual disturbances

📄 Stop Use and Ask a Doctor If 30 words ▾

Stop use and ask a doctor if: you experience chest pain, fainting, sudden vision or hearing loss an erection lasts longer than 4 hours (priapism). This is a medical emergency.

📄 Keep Out of Reach of Children 17 words ▾

Contraindications Not for use in pregnant or breastfeeding women Not for use in children under 18 years

📄 Package Label / Principal Display Panel 7 words ▾

PRINCIPAL DISPLAY PANEL 01 02 03 04

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 3 other package presentations of this same product, including 1 patch (84778-0089-01), 4 patches (84778-0089-03), 8 patches (84778-0089-04). 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?
Guangzhou Yixin Cross-border E-commerce Co., Ltd. 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.
← 84778-0088-01 · Guangzhou 84778-0090-01 · Guangzhou →
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.