Home › NDC Lookup › Ingredients › Panax Ginseng Root Extract 7% › 85277-0002-01
Rhtalgorism Delay Sprays for Men Panax Ginseng Root Extract 7% .07 g/100mL; .07 g/100mL; .07 g/100mL; 1 g/100mL; 7 g/100mL; .7 g/100mL; .04 g/100mL Liquid, 6 mL — NDC 85277-0002-01 package photo

Rhtalgorism Delay Sprays for Men Panax Ginseng Root Extract 7% .07 g/100mL; .07 g/100mL; .07 g/100mL; 1 g/100mL; 7 g/100mL; .7 g/100mL; .04 g/100mL Liquid, 6 mL

by Guangdong Meizhiyuan Biotechnology Co., Ltd. · 6 mL in 1 BOTTLE (85277-002-01)
NDC 85277-0002-01
🏷️ FDA NDC (as labeled) 85277-002-01 billing pads the product segment with a zero
This package
Contains6 mL Pack sizes3 compare ↓
Also comes in: 12 ml 85277-0002-02 30 ml 85277-0002-03
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) 85277-002-01
Product NDC 85277-002
11-digit billing NDC 85277000201
UNII Z608183YD0, BOW48C81XP, 1D5HJN5DG4, 1BEM3U6LQQ, CUQ3A77YXI, V1IA3S3CUS +1 more
Application # 505G(a)(3)
SPL Set ID 4fe00413-0938-2c82-e063-6294a90a3b1f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-20
Route TOPICAL
Dosage form LIQUID
Substance CERVUS ELAPHUS VELVET; PIPER METHYSTICUM ROOT; EPIMEDIUM BREVICORNU TOP; REHMANNIA GLUTINOSA ROOT; ASIAN GINSENG; CNIDIUM MONNIERI FRUIT; POLYGONATUM ODORATUM ROOT
Why two NDCs? The FDA registers this code as 85277-002-01 — 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 → 85277-0002-01. 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

LabelerGuangdong Meizhiyuan Biotechnology Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85277
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio2 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?

This is a topical spray marketed as an OTC monograph product for men. It contains a blend of herbal extracts, including Asian ginseng, deer antler velvet, cnidium, epimedium, kava root, polygonatum, and rehmannia. These plant-derived ingredients are traditionally used in herbal products intended to support male sexual function and performance. The spray is applied to the skin rather than taken by mouth.

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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 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.

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

The official label also statesALCOHOL BUTYLENE GLYCOL 1,2-HEXANEDIOL 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.

💲 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.
Try another pack size: 12 ml 30 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rhtalgorism Delay Sprays for Men .07 g/100mL; .07 g/100mL; .07 g/100mL; 1 g/100mL; 7 g/100mL; .7 g/100mL; .04 g/100mLthis 85277-0002-01 Guangdong 6 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

🏛️
2026
On the market since
Apr 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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
85277-0002-01 You're viewing this 6 mL in 1 BOTTLE (85277-002-01) 2026-04-20 Active
85277-0002-02 12 mL in 1 BOTTLE (85277-002-02) 2026-04-20 Active
85277-0002-03 30 mL in 1 BOTTLE (85277-002-03) 2026-04-20 Active

You're viewing the smallest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 85277-0002-01?
NDC 85277-0002-01 contains 6 mL — 6 ml in 1 bottle.
What is the difference between NDC 85277-0002-01 and NDC 85277-0002-02?
Both are Rhtalgorism Delay Sprays for Men Panax Ginseng Root Extract 7% .07 g/100mL; .07 g/100mL; .07 g/100mL; 1 g/100mL; 7 g/100mL; .7 g/100mL; .04 g/100mL Liquid — the drug itself is identical. NDC 85277-0002-01 is the 6 mL package, while NDC 85277-0002-02 is the 12 ml package.
What NDC number is used to bill for this package of Rhtalgorism Delay Sprays for Men Panax Ginseng Root Extract 7% .07 g/100mL; .07 g/100mL; .07 g/100mL; 1 g/100mL; 7 g/100mL; .7 g/100mL; .04 g/100mL Liquid?
Bill NDC 85277-0002-01 — the 11-digit billing format is 85277000201. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 85277-002-01, 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: 85277-0002-01, written without dashes as 85277000201. 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 85277-0002-01, the first segment (85277) is the labeler code FDA assigned to Guangdong Meizhiyuan Biotechnology Co., Ltd.; 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 Guangdong Meizhiyuan Biotechnology Co., Ltd.. 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 2 other package presentations of this same product, including 12 ml (85277-0002-02), 30 ml (85277-0002-03). 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?
Guangdong Meizhiyuan Biotechnology 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.

📄 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 21 words ▾

Its main function is to reduce local sensitivity, thereby prolonging sexual intercourse time to a certain extent and improving sexual satisfaction

⏱️ Dosage and Administration 133 words ▾

1.Timing: For best results, apply 10 to 20 minutes before intimacy. 2.Application Apply 0.2 m of this product by spraying it onto the coronal sulcus area. (Typically one or two presses of the spray nozle wildispense a 0.2 m dose.

If you fnd it dificultto control the dosage,you may dip a cotton swab into the liquid and apply it in a circular motionaround the coronal sulcus.) Then, pull the foreskin back over the area to allow the liquid to be fully absorbed. 3.Absorption: Allow It to air dry naturally. No need to wipe or rinse oft.

You wll appreciate Its non-greasy feel. 4.Application area: Apply this product to the coronal sulcus and penis body, do not spray on theurethral opening, otherwise it will reduce the efficacy 5.Cleanliness: Wash hands before and after use

⚠️ Warnings 108 words ▾

1.Consult Your Doctor. Consult your doctor before use if you have heart disease, high blood pressure, or any serious medical condition. 2.Not a Contraceptive This product is not a contraceptive and does not protect against sexually transmitted diseases.

3. For Adults Only: For adult use only 4. Do Not Share: Do not share this product with others to prevent cross-contamination.

5.individual Results May Vary. intended Use: This productis intended as an ald for personal welless and is not meantto diagnose, treat, cure, or prevent any disease. For any health concerns, seek professional medical advice. if you have any questions during use, please email the brand's official mailbox: [email protected]

🧪 Active Ingredient 33 words ▾

PIPER METHYSTICUM ROOT EXTRACT 0.07% EPIMEDIUM BREVICORNUM EXTRACT 0.07% CERVUS ELAPHUS EXTRACT 0.07% PANAX GINSENG ROOT EXTRACT 7.00% CNIDIUM MONNIERI FRUIT EXTRACT 0.7% POLYGONATUM OFFICINALE RHIZOME/ROOT EXTRACT 0.035% REHMANNIA CHINENSIS ROOT EXTRACT 1.4%

🧪 Inactive Ingredients 5 words ▾

ALCOHOL BUTYLENE GLYCOL 1,2-HEXANEDIOL water

🎯 Purpose 4 words ▾

Rhtalgorism Male Delay Spray

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85277-0001-01 · Guangdong 85278-0251-20 · Wellmetech →
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.