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NOAVIA PORE FIRMING SERUM FIELD MUSHROOM,HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER 3 g/100mL; 2 g/100mL Liquid, 30 mL — NDC 85212-0013-01 package photo

NOAVIA PORE FIRMING SERUM FIELD MUSHROOM,HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER 3 g/100mL; 2 g/100mL Liquid, 30 mL

by Beijing JUNGE Technology Co., Ltd. · 30 mL in 1 BOTTLE (85212-0013-1)
NDC 85212-0013-01
🏷️ FDA NDC (as labeled) 85212-0013-1 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) 85212-0013-1
Product NDC 85212-0013
11-digit billing NDC 85212001301
UNII 19988ORO24, 8FP93ED6H2
Application # 505G(a)(3)
SPL Set ID 2f06ddef-a6ac-c5bc-e063-6394a90af451
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-09-01
Route EXTRACORPOREAL
Dosage form LIQUID
Substance FIELD MUSHROOM; HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER
Why two NDCs? The FDA registers this code as 85212-0013-1 — 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 → 85212-0013-01. 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 marketedSep 2024
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?

Noavia Pore Firming Serum is a liquid skincare product applied to the skin. It contains field mushroom and witch hazel leaf water as active ingredients. These botanical ingredients are commonly used in skincare products for their astringent and toning properties, typically intended to help tighten the appearance of pores and provide a firming effect. This is an over-the-counter monograph drug marketed under FDA's established rule-book for skincare products in this category.

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.

💊 What it looks like

ShapeFreeform
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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.

  • 2 mL / 100 mL 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.
  • 73.2 mL / 100 mL 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.
  • 5 mL / 100 mL 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.
  • 0.5 mL / 100 mL UNII YPX537PA31
    A plant extract from chrysanthellum indicum used as a natural colorant or flavoring agent in medicines. It may help create visual appeal or subtle taste characteristics in the formulation.
  • 3 mL / 100 mL UNII O9ECF2PL1F
    A plant extract from chrysanthemum flowers used as a natural colorant and flavoring agent. It may provide color, taste, or aroma to the medicine while serving as a botanical ingredient in the formulation.
  • 5 mL / 100 mL UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • 0.5 mL / 100 mL UNII O3E12ZLW5T
    A plant extract from houttuynia cordata, an herb used in traditional Asian medicine. It may serve as a natural flavoring agent or botanical additive in the formulation.
  • 2 mL / 100 mL UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • 0.1 mL / 100 mL UNII 3TF9Z1U73O
    A plant-derived ingredient from the prickly pear cactus stem. It acts as a binder and thickener to help hold the medicine together and improve its texture.
  • 0.1 mL / 100 mL UNII 7M7E9A2C8J
    A plant extract from tree peony root used in traditional medicine formulations. It may function as a natural flavoring agent, colorant, or botanical ingredient to support the product's overall composition.
  • 0.5 mL / 100 mL UNII D5J3623SV2
    Portulaca oleracea is a plant extract used in medicines as a natural ingredient. It may function as an antioxidant or skin-conditioning agent in topical formulations.
  • 0.1 mL / 100 mL 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.
  • 1 mL / 100 mL 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.
  • 1 mL / 100 mL UNII 4938BNS0GU
    A fungal extract from tremella fuciformis, a jelly-like mushroom. It acts as a thickener, emulsifier, and skin-conditioning agent in topical formulations to improve texture and moisture retention.
  • 1 mL / 100 mL UNII QT8A71T9BM
    A plant extract from verbena, used as a flavoring agent to add taste or aroma to the medicine and make it more palatable for patients.

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

The official label also statesAQUA BUTYLENE GLYCOL GLYCERIN SPIRAEA ULMARIA EXTRACT HYDROXYACETOPHENONE 1,2-HEXANEDIOL TREMELLA FUCIFORMIS SPOROCARP EXTRACT VERBENA OFFICINALIS EXTRACT BUTYLENE GLYCOL PORTULACA OLERACEA EXTRACT CHRYSANTHELLUM INDICUM EXTRACT HOUTTUYNIA CORDATA EXTRACT OPUNTIA STREPTACANTHA STEM EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT PAEONIA SUFFRUTICOSA ROOT 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 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.
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
Noavia Pore Firming Serum 3 g/100mL; 2 g/100mLthis 85212-0013-01 Beijing 30 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

🏛️
2024
On the market since
Sep 2024
📍
2026
Currently FDA-listed
2 years 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
85212-0013-01 You're viewing this 30 mL in 1 BOTTLE (85212-0013-1) 2024-09-01 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 85212-0013-1, 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: 85212-0013-01, written without dashes as 85212001301. 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 85212-0013-01, the first segment (85212) is the labeler code FDA assigned to Beijing JUNGE Technology Co., Ltd.; the middle segment (0013) 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 29 words ▾

BOTANICAL PURITY FOR A YOUTHFUL COMPLEXION SOOTHES, PROTECTS, AND BALANCES SENSITIVE SKIN It relieves dry, flaky skin and protects against irritation and harmful microbes, restoring balance to your skin.

⏱️ Dosage and Administration 1 words ▾

30ml/1fl.oz

⚠️ Warnings 13 words ▾

For external use only. Keep out of reach of children.Avoid contact with eyes.

🧪 Active Ingredient 11 words ▾

FOMES OFFICINALIS (MUSHROOM) EXTRACT HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT SODIUM HYALURONATE

🧪 Inactive Ingredients 39 words ▾

AQUA BUTYLENE GLYCOL GLYCERIN SPIRAEA ULMARIA EXTRACT HYDROXYACETOPHENONE 1,2-HEXANEDIOL TREMELLA FUCIFORMIS SPOROCARP EXTRACT VERBENA OFFICINALIS EXTRACT BUTYLENE GLYCOL PORTULACA OLERACEA EXTRACT CHRYSANTHELLUM INDICUM EXTRACT HOUTTUYNIA CORDATA EXTRACT OPUNTIA STREPTACANTHA STEM EXTRACT SCUTELLARIA BAICALENSIS ROOT EXTRACT PAEONIA SUFFRUTICOSA ROOT EXTRACT

🎯 Purpose 16 words ▾

EFFECTIVE BLACKHEAD AND PORE CARE BOTANICAL PURITY FOR A YOUTHFUL COMPLEXION INTENSE HYDRATION AND SKIN RESILIENCE

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85212-0012-01 · Beijing 85212-0014-01 · 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.