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Arthcal VULVA BALM BEESWAX,SHEA BUTTER,GRAPE SEED 5 g/100g; 5 g/100g; 5 g/100g Cream, 50 g

by Beijing JUNGE Technology Co., Ltd. · 50 g in 1 CAN (85212-0024-1)
NDC 85212-0024-01
🏷️ FDA NDC (as labeled) 85212-0024-1 billing pads the package segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 85212-0024-1
Product NDC 85212-0024
11-digit billing NDC 85212002401
UNII 2ZA36H0S2V, 930MLC8XGG, K49155WL9Y
Application # 505G(a)(3)
SPL Set ID 2f305967-207b-6da9-e063-6294a90a571c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-01-10
Route EXTRACORPOREAL
Dosage form CREAM
Substance BEESWAX; GRAPE SEED OIL; SHEA BUTTER
Why two NDCs? The FDA registers this code as 85212-0024-1 — a 5-4-1 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 package segment → 85212-0024-01. 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

LabelerBeijing JUNGE Technology Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85212
First marketedJan 2025
Product typeHuman Otc Drug
Portfolio34 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?

Arthcal Vulva Balm is an over-the-counter cream marketed under FDA's OTC monograph rules for topical skin care. It contains beeswax, shea butter, and grape seed oil, which are commonly used as emollients and moisturizers in products applied to the skin. These ingredients are typically included to help soften and protect the skin barrier.

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.

  • 63 g / 100 g 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.
  • 0.2 g / 100 g UNII 7S95JTU3F1
    Artemisia scoparia is a plant material used in some pharmaceutical formulations. It may serve as a natural flavoring agent, colorant, or botanical extract component in the medicine.
  • 0.5 g / 100 g UNII 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • 1.5 g / 100 g UNII 344821WD61
    Emu oil is a natural fat derived from emu birds, used in some medicines as an emollient and penetration enhancer to help active ingredients absorb through the skin and soften the formulation.
  • 2 g / 100 g UNII 3Q9L08K71N
    Evening primrose oil is a plant-based oil extracted from evening primrose seeds. It's used in medications as an emollient and to improve texture and absorption in soft capsule formulations.
  • 5 g / 100 g UNII Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • 0.5 g / 100 g UNII JA69U4B4XI
    A plant-based oil derived from avocado that has been chemically treated to make it solid and stable. It serves as a binder and filler to hold tablet ingredients together and add volume to the formulation.
  • 0.5 g / 100 g UNII JY81OXM1OM
    A plant-based oil from coconut that has been chemically treated to solidify it. It acts as a binder and filler to help hold tablet ingredients together and give the pill its shape and firmness.
  • 0.5 g / 100 g UNII 15E7C67EE8
    A natural seaweed extract used as a thickener and gelling agent in medicines. It helps create the right texture and consistency in liquid or semi-solid formulations.
  • 0.2 g / 100 g UNII SA8AR2W4ER
    A natural oil extracted from chamomile flower tops, used as a flavoring and fragrance agent to improve taste and aroma in medicines.
  • 3.4 g / 100 g 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.
  • 0.5 g / 100 g UNII 7TRV45YZF7
    A plant extract from Japanese knotweed root used as a natural ingredient. It functions as an antioxidant and preservative to help maintain product stability and shelf life.
  • 0.5 g / 100 g UNII 969IQC5YJU
    A natural plant extract from the rugosa rose flower. It's used in formulations as a fragrance, flavor, or natural colorant to improve the taste, smell, or appearance of the medicine.
  • 0.2 g / 100 g UNII IJ67X351P9
    A natural plant extract from rosemary leaves used as a preservative to help prevent oils and fats in the medicine from spoiling or becoming rancid during storage.
  • 0.5 g / 100 g UNII L497I37F0C
    Royal jelly is a creamy, nutrient-rich secretion produced by honeybees. In medications, it serves as a natural sweetener, flavor enhancer, and ingredient that may improve taste and palatability of oral formulations.
  • 0.5 g / 100 g UNII 7J95K7ID2S
    A plant extract from the roots of Chinese skullcap, used as a natural coloring agent and to add mild flavor to medicines. It may also help preserve the product's stability.
  • 5 g / 100 g UNII R9N3379M4Z
    Sunflower seed is a plant-derived ingredient used as a filler and source of oil in medications. It helps add bulk to the formulation and may serve as a natural binding or lubricating component.
  • 0.5 g / 100 g 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.

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

The official label also statesAQUA SUNFLOWER SEED OIL MEL OLIVE FRUIT OIL EVENING PRIMROSE OIL EMU OIL TOCOPHEROL HYDROGENATED COCONUT OIL HYDROGENATED AVOCADO OIL HIPPOPHAE RHAMNOIDES OIL ROYAL JELLY EXTRACT ROSA RUGOSA FLOWER EXTRACT CENTELLA ASIATICA EXTRACT POLYGONUM CUSPIDATUM ROOT EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT ARTEMISIA SCOPARIA EXTRACT

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
Arthcal VULVA BALM 5 g/100g; 5 g/100g; 5 g/100gthis 85212-0024-01 Beijing 50 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

🏛️
2025
On the market since
Jan 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85212-0024-01 You're viewing this 50 g in 1 CAN (85212-0024-1) 2025-01-10 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 — Not published for this NDC No photo available yet for this listing.
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 85212-0024-1, 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: 85212-0024-01, written without dashes as 85212002401. 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 85212-0024-01, the first segment (85212) is the labeler code FDA assigned to Beijing JUNGE Technology Co., Ltd.; the middle segment (0024) 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 Beijing JUNGE Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Beijing JUNGE Technology 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 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 25 words ▾

Clean Hands: Ensure your hands are clean and dry. Apply Directly: Apply an appropriate amount of the productectly. Massage to Absorb:Gently massage until fully absorbed.

⏱️ Dosage and Administration 1 words ▾

50g(1.76oz)

⚠️ Warnings 74 words ▾

1. For Extemal Use Only. 2. Avoid Direct Contact with Eyes. 3. If the product gets into your eyes, rinse immediately with plenty of water. 4. Ensure skin is not broken or severely irritated before use. 5. If any discomfort or allergic reaction occurs, discontinue use immediately and consult a doctor.6. TIP For optimal results, maintain daily use and increase frequency as needed based on personal requirements. 7. Keep Out of Reach of Children.

🧪 Inactive Ingredients 54 words ▾

AQUA SUNFLOWER SEED OIL MEL OLIVE FRUIT OIL EVENING PRIMROSE OIL EMU OIL TOCOPHEROL HYDROGENATED COCONUT OIL HYDROGENATED AVOCADO OIL HIPPOPHAE RHAMNOIDES OIL ROYAL JELLY EXTRACT ROSA RUGOSA FLOWER EXTRACT CENTELLA ASIATICA EXTRACT POLYGONUM CUSPIDATUM ROOT EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT ARTEMISIA SCOPARIA EXTRACT

🎯 Purpose 8 words ▾

Address dryness, discomfort, and sensitivity in delicate areas.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85212-0023-01 · Beijing 85212-0028-01 · Beijing →
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.