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DRMITSUI VAGINAL PROBIOTICS 5 g/100g; 3 g/100g; 3 g/100g Gel — NDC 87267-0010-01 package photo

DRMITSUI VAGINAL PROBIOTICS 5 g/100g; 3 g/100g; 3 g/100g Gel

by YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED · 7 TUBE in 1 BOX (87267-010-01) / 3 g in 1 TUBE
NDC 87267-0010-01
🏷️ FDA NDC (as labeled) 87267-010-01 billing pads the product segment with a zero
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) 87267-010-01
Product NDC 87267-010
11-digit billing NDC 87267001001
UNII TZ0BE8I3MW, M08917G08Z, 8MXU1P42J0
UPC 4573638420534
Application # 505G(a)(3)
SPL Set ID 5172ff86-8195-2296-e063-6294a90acf8f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-05-10
Route TOPICAL
Dosage form GEL
Substance ROSA RUGOSA FLOWER BUD; PORTULACA OLERACEA SEED; CENTELLA ASIATICA ROOT
Why two NDCs? The FDA registers this code as 87267-010-01 — 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 → 87267-0010-01. 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

LabelerYIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code87267
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio9 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 an over-the-counter topical gel marketed under FDA monograph rules for vaginal use. It contains three plant-derived ingredients: Centella asiatica root, Portulaca oleracea seed, and Rosa rugosa flower bud. These botanical extracts are commonly included in products intended to support vaginal comfort and skin health in the intimate area. The gel formulation is applied topically to the vaginal region.

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 02LN7O412C
    A natural sugar made from plant sources, used as a sweetener and texturizer in medicines to improve taste and give the product body and consistency.
  • 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 1O6C93RI7Z
    Dexpanthenol is a naturally derived compound related to B vitamins. It acts as a humectant and skin conditioning agent, helping the medicine absorb moisture and maintain softness in topical formulations.
  • UNII 8VF8J08EB6
    A natural extract from longan fruit seeds used as a filler and binding agent in formulations. It helps hold tablet or capsule ingredients together and adds bulk to the medicine.
  • UNII 01KM283D85
    A derivative of fructose combined with phenylhydrazine, this chemical compound functions as a reference standard or analytical marker in pharmaceutical testing and quality control to verify product identity and purity.
  • UNII G97P6S66E9
    A sugar alcohol derivative made by combining glucose and mannitol. It acts as a filler and sweetener in tablets and capsules, adding bulk to the medicine and providing a slightly sweet taste without affecting the active ingredient's function.
  • UNII YSE9PPT4TH
    Hyaluronate sodium is a natural carbohydrate that holds moisture. It's used in medicines as a lubricant, thickener, and moisture-retaining agent to improve texture and delivery of the active ingredient.
  • UNII S270N0TRQY
    Hyaluronic acid is a naturally occurring substance found in skin and joints. In medicines, it acts as a moisturizer and thickening agent to improve texture and help the product spread smoothly.
  • UNII JOS53KRJ01
    Inulin is a fiber derived from plants like chicory root. It acts as a filler and binder in medicines to add bulk and help hold tablets together.
  • UNII 67I334IX2M
    Isomaltose is a simple sugar made from starch. It's used in medicines as a sweetener and filler to improve taste and add bulk to the formulation.
  • UNII 02833ISA66
    Levoglucose is a naturally occurring sugar derived from starch. In medicines, it typically acts as a filler to add bulk and volume, and as a sweetener or binding agent to help hold tablet ingredients together.
  • 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 3M4G523W1G
    Silver is a metallic element used in some medications as an antimicrobial agent in topical formulations. It helps prevent bacterial growth on wound dressings and certain skin preparations.
  • UNII WN66R7GL93
    A modified form of hyaluronic acid, a naturally occurring substance that holds water. Used as a thickener, lubricant, and moisture-retaining agent in formulations, especially in topical or injectable products.
  • UNII 788QAG3W8A
    A synthetic polymer that combines polyethylene glycol, glycidyl ether, and sodium hyaluronate. It acts as a thickener and film-former in topical products, helping maintain texture and improve how the medicine spreads on skin.
  • 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.

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

The official label also statesWater, Longan (Euphoria Longana) FruitExtract, Glucose, Propylene Glycol, IsomaltOligosaccharide, Fructooligosaccharide,Inulin, Sodium Hyaluronate, HydrolysedSodium Hyaluronate, Hyaluronic Acid,Hydrolysed Hyaluronic Acid, AcetylatedSodium Hyaluronate, Cross-linked SodiumHyaluronate Polymer, Pro-vitamin B5,Rosa Rugosa Flower Water, CentellaAsiatica Extract, Purslane (PortulacaOleracea) Extract, Silver Lons, Carbomer,Triethanolamine.

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Drmitsui Vaginal Probiotics 5 g/100g; 3 g/100g; 3 g/100gthis 87267-0010-01 YIYANGYUAN 7 tubes — — 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
May 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
87267-0010-01 You're viewing this 7 TUBE in 1 BOX (87267-010-01) / 3 g in 1 TUBE 2026-05-10 Active

🧭 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 87267-010-01, 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: 87267-0010-01, written without dashes as 87267001001. 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 87267-0010-01, the first segment (87267) is the labeler code FDA assigned to YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED; the middle segment (0010) 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 YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED 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 42 words ▾

By forming a protective gel film on thevaginal wall, the product physically isolatesthe vaginal wall from external bacteria,thereby preventing the colonization ofpathogenic microorganisms. It is indicatedfor the adjunctive treatment of chroniccervicitis and vaginitis. The product issupplied non-sterile and is for single-use only.

⏱️ Dosage and Administration 32 words ▾

Clean the perineal area before use. Assumea squatting or lying position, relax yourbody, gently insert the applicator into thevagina, and gently dispense the gel. Useone applicator per night for a 7-daytreatment cycle.

⚠️ Warnings 11 words ▾

For external use only. Discontinue useimmediately if an allergic reaction occurs.

🧪 Active Ingredient 11 words ▾

Rosa Rugosa Flower Water Centella Asiatica Extract Purslane (Portulaca Oleracea) Extract

🧪 Inactive Ingredients 36 words ▾

Water, Longan (Euphoria Longana) FruitExtract, Glucose, Propylene Glycol, IsomaltOligosaccharide, Fructooligosaccharide,Inulin, Sodium Hyaluronate, HydrolysedSodium Hyaluronate, Hyaluronic Acid,Hydrolysed Hyaluronic Acid, AcetylatedSodium Hyaluronate, Cross-linked SodiumHyaluronate Polymer, Pro-vitamin B5,Rosa Rugosa Flower Water, CentellaAsiatica Extract, Purslane (PortulacaOleracea) Extract, Silver Lons, Carbomer,Triethanolamine.

🎯 Purpose 9 words ▾

VAGINAL HEALTH UNPLEASANT ODOR VAGINAL MOISTURIZER PH BALANCE RESTORER·

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87267-0004-01 · YIYANGYUAN 87267-0011-01 · YIYANGYUAN →
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.