Home › NDC Lookup › 87947-0001-01
Pharmlitalia Vaginal Symptoms Relief Borax,Calendula officinalis,Hydrastis canadensis,Olive Extract 3 [hp_X]/g; 1 [hp_X]/g; 5 [hp_X]/g; 3 [hp_X]/g Gel, 12.1 g — NDC 87947-0001-01 package photo

Pharmlitalia Vaginal Symptoms Relief Borax,Calendula officinalis,Hydrastis canadensis,Olive Extract 3 [hp_X]/g; 1 [hp_X]/g; 5 [hp_X]/g; 3 [hp_X]/g Gel, 12.1 g

by Guangzhou Trading Financing Union LLC · 12.1 g in 1 APPLICATOR (87947-001-01)
NDC 87947-0001-01
🏷️ FDA NDC (as labeled) 87947-001-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 10, 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) 87947-001-01
Product NDC 87947-001
11-digit billing NDC 87947000101
UNII 91MBZ8H3QO, PFR03EBU0H, ZW3Z11D0JV, 2O4553545L
SPL Set ID ad63f5aa-dfa7-4773-bec2-12ccf8181f95
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-18
Route VAGINAL
Dosage form GEL
Substance SODIUM BORATE; CALENDULA OFFICINALIS WHOLE; GOLDENSEAL; OLEUROPEIN
Why two NDCs? The FDA registers this code as 87947-001-01 — 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 → 87947-0001-01. 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

LabelerGuangzhou Trading Financing Union LLC
Labeler code87947
First marketedAug 2026
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.

🩺 Clinical

🧪 What is this product?

This is an unapproved homeopathic vaginal gel containing sodium borate, calendula, goldenseal, and oleuropein. In homeopathic practice, these ingredients are traditionally used to address vaginal discomfort and irritation. Homeopathic products are marketed based on traditional use and are not evaluated by the FDA for safety or effectiveness. The potencies listed indicate this product follows homeopathic preparation methods rather than conventional pharmaceutical standards.

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 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 C7X957O5YS
    Curcuma aromatica root is a plant-derived powder that adds color and mild flavor to medicines. It may serve as a natural colorant or help improve the product's appearance and taste.
  • UNII J9130AL5GC
    A plant extract from zedoary, a ginger-family spice. It serves as a natural colorant and flavoring agent in the medicine, contributing to the product's appearance and taste.
  • UNII 6UYK2W1W1E
    A natural oil extracted from olives. It acts as an emollient and lubricant in formulations, helping to soften ingredients and improve how the medicine spreads or flows.
  • UNII 82LKS4QV2Y
    Poliglusam is a synthetic polymer made from glucose units linked together. It works as a binder and thickening agent to help hold the medicine's ingredients together and control how quickly the drug dissolves.
  • 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 X8KX602M5L
    Sophora flavescens is a plant extract used in medicines as a natural thickening agent and skin-conditioning ingredient. It helps adjust the medicine's texture and may support formulation stability.
  • UNII 66ZQ85S65H
    A plant-derived substance from the roots of Sparganium stoloniferum, used in some formulations as a natural binder or thickening agent to help hold ingredients together and give the medicine its solid form.

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

The official label also statesChamomilla Recutita (Chamomile) Extract, Chitosan, Collagen Peptide,Curcuma Zedoaria Extract, Oxygenated Olive Oil, Radix Curcumae Extract, Rhizoma Sparganii Extract, Sodium Hyaluronate, Sophora Flavescens (Kuh-seng) Extract. *Claims based on traditional homeopathic practice and not on modern scientific evidence.

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
Pharmlitalia Vaginal Symptoms Relief 3 [hp_X]/g; 1 [hp_X]/g; 5 [hp_X]/g; 3 [hp_X]/gthis 87947-0001-01 Guangzhou 12.1 g — — 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
Aug 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
87947-0001-01 You're viewing this 12.1 g in 1 APPLICATOR (87947-001-01) 2026-08-18 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Pharmlitalia Vaginal Symptoms Relief Borax,Calendula officinalis,Hydrastis canadensis,Olive Extract 3 [hp_X]/g; 1 [hp_X]/g; 5 [hp_X]/g; 3 [hp_X]/g GEL is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

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 "Unapproved Homeopathic". 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 87947-001-01, 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: 87947-0001-01, written without dashes as 87947000101. 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 87947-0001-01, the first segment (87947) is the labeler code FDA assigned to Guangzhou Trading Financing Union LLC; the middle segment (0001) 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 Guangzhou Trading Financing Union LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Trading Financing Union 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.

📄 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
🎯 Indications and Usage 13 words ▾

Uses For the temporary relief of minor vaginal discomfort and feelings of irritation.

⏱️ Dosage and Administration 40 words ▾

Directions • adults: insert one (1) applicator vaginally at bedtime • use once daily for up to 7 consecutive nights • do not use more than one applicator in any 24-hour period • children under 12 years: ask a doctor

⚠️ Warnings ~1 min read ▾

Warnings For vaginal use only . Do not swallow; For adult use only. Donot use: • if you have never had vaginal symptoms before • if you are allergic to any of the ingredients in this product • if you have fever, chills, abdominal pain, or pelvic pain • if you have abnormal vaginal bleeding • if the applicator wrapper or seal is damaged, torn, or shows incomplete seals Ask a doctor before use if you have: • diabetes, a weakened immune system, or a history of recurrent vaginal infections • a serious medical condition or are under medical supervision • symptoms that have lasted more than 7 days before starting use When using this product: • you may experience mild burning, itching, or irritation at the application site • do not use tampons, douches, spermicides, or other vaginal products • this product may damage condoms and diaphragms and reduce their effectiveness • avoid contact with eyes Stop use and ask a doctor if: • symptoms do not improve within 3 days • symptoms last more than 7 days • symptoms worsen or return after completion • new symptoms develop, including fever, rash, pelvic pain, nausea, or unusual bleeding • severe burning, swelling, or rash occurs at the application site If pregnant or breastfeeding , ask a healthcare professional before use.

Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

🧪 Active Ingredient 41 words ▾

Active Ingredients (per applicator)....................................Purpose Borax 3X HPUS (Sodium Borate) Homeopathic* Calendula officinalis 1X HPUS Homeopathic* Hydrastis canadensis 5X HPUS Homeopathic* Olive Extract (Oleuropein) 3X HPUS Homeopathic* *HPUS indicates the active ingredients are in the official Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 38 words ▾

Inactive Ingredients Chamomilla Recutita (Chamomile) Extract, Chitosan, Collagen Peptide,Curcuma Zedoaria Extract, Oxygenated Olive Oil, Radix Curcumae Extract, Rhizoma Sparganii Extract, Sodium Hyaluronate, Sophora Flavescens (Kuh-seng) Extract. *Claims based on traditional homeopathic practice and not on modern scientific evidence.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87943-0085-20 · DW 87949-0001-01 · Foshan →
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.