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Hazel Perineal Healing Foam Witch 50 g/100mL Liquid, 100 mL — NDC 85448-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Hazel Perineal Healing Foam Witch 50 g/100mL Liquid, 100 mL — NDC 85448-001-01 (Billing 85448-0001-01)

by Jiangsu Senwo Medical Technology Co., Ltd. · 100 mL in 1 BOTTLE

This is a package of 100 mL of Hazel Perineal Healing Foam Witch 50 g/100mL Liquid from Jiangsu Senwo Medical Technology Co., Ltd., marketed since Jul 2024 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 85448-0001-01
🏷️ FDA NDC (as labeled) 85448-001-01 billing pads the product segment with a zero
This package
Contains100 mL Pack sizes2 compare ↓
Main listing for product 85448-001 · Also comes in: 150 ml 85448-001-02
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 85448-001-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85448 labeler · 001 product · 01 package
Package marketed since
Jul 4, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8544800101 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85448-001-01
Product NDC 85448-001
11-digit billing NDC 85448000101
RxCUI 2166922
UNII 101I4J0U34
Application # M015
SPL Set ID 314b75cb-affe-a248-e063-6294a90a47b7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-07-04
Route TOPICAL
Dosage form LIQUID
Substance WITCH HAZEL
Quick answers
  • RxCUI (RxNorm): 2166922
Why two NDCs? The FDA registers this code as 85448-001-01 — 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 → 85448-0001-01. 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.

Clinical

🧪 What is this product?

This is a topical liquid foam containing witch hazel, an OTC monograph product intended for use on the perineal area. Witch hazel is commonly used in skincare products for its astringent properties and is typically applied to the skin to help with minor irritation and cleansing. The product is formulated as a foam for topical application and comes in a 50 g per 100 mL concentration.

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.

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: 150 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
85448-0001-01 You're viewing this Main listing 100 mL in 1 BOTTLE 2024-07-04 — Active
85448-0001-02 85448-001-02 150 mL in 1 BOTTLE 2024-07-04 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 100 mL — 100 ml in 1 bottle.
How does this package differ from NDC 85448-0001-02?
Both are Hazel Perineal Healing Foam Witch 50 g/100mL Liquid — the drug itself is identical. This page's package is the 100 mL one, while NDC 85448-0001-02 is the 150 ml package.
What NDC number is used to bill for this package of Hazel Perineal Healing Foam Witch 50 g/100mL Liquid?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
The Pharma C Company Medicated Foam with Witch Hazel 500 mg/mL 55239-0358-00 Kleen 210 ml — — FDA listed —
frida mom Perineal Healing .5 g/g 72705-0150-02 Fridababy, 1 bottle — — FDA listed —
Hazel Perineal Healing Foam 50 g/100mLthis 85448-0001-01 Jiangsu 100 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
Jul 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.

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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • 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 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII RA96B954X6
    Erythritol is a sugar alcohol derived from fermented fruits or grains. It's used as a sweetener and bulking agent in medicines to improve taste without adding significant calories.
  • 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.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • UNII 6DRV3D37XS
    A plant extract from Chinese lizard's tail (Saururus chinensis), used in traditional herbal preparations. It serves as an active botanical ingredient that may provide therapeutic properties, though its specific formulation role in this product depends on the medicine's intended use.
  • UNII NCX1UU2D33
    Sodium lauroyl glutamate is a mild cleanser derived from coconut oil and the amino acid glutamate. In medicines, it acts as a surfactant and emulsifier to help mix oily and watery ingredients and improve how the product spreads or dissolves.
  • UNII 632GS99618
    Sodium lauroyl sarcosinate is a mild, plant-derived cleaning agent used in medicines as a surfactant and emulsifier. It helps mix oil and water-based ingredients and may aid tablet disintegration.
  • UNII 7S7TV2F4XC
    A plant extract from Stephania tetrandra, a vine used traditionally in herbal preparations. In medications, it may serve as an active botanical ingredient or provide binding and consistency properties to the formulation.
  • UNII 39981FM375
    A plant extract from the common dandelion, used as a natural flavoring agent or botanical ingredient to add taste and plant-derived components to the medicine.
  • 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.
  • 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 C12-18 ALKYL GLUCOSIDE SODIUM LAUROYL SARCOSINATE SODIUM LAUROYL GLUTAMATE COCAMIDOPROPYL BETAINE ERYTHRITOL BUTYLENE GLYCOL ALCOHOL HYDROXYACETOPHENONE 1,2-HEXANEDIOL PHENOXYETHANOL TOCOPHEROL SAURURUS CHINENSIS LEAF/ROOT EXTRACT TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT STEPHANIA TETRANDRA EXTRACT MENTHA HAPLOCALYX OIL CITRIC ACID PEG-40 HYDROGENATED CASTOR OIL

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.

Manufacturer & labeler

LabelerJiangsu Senwo Medical Technology Co., Ltd.
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code85448
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Jiangsu Senwo Medical Technology Co., Ltd. labeler code 85448

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.

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Helps relieve pain and swelling from hemorrhoids and childbirth.

⏱️ Dosage and Administration 40 words ▾

When using this product m Avoid contact with eyes.lf contact occurs.rinsethoroughly with water..Do not exceed the recommended daily dosage unlessdirected by a doctor m Do not put this product into the rectum by using fingeror any mechanical device or applicator.

⚠️ Warnings 4 words ▾

For external use only

📦 Storage and Handling 10 words ▾

Other informationm Store at room temperature Single use per wipe

🧪 Active Ingredient 3 words ▾

Witch Hazel 50%

🧪 Inactive Ingredients 41 words ▾

Water C12-18 ALKYL GLUCOSIDE SODIUM LAUROYL SARCOSINATE SODIUM LAUROYL GLUTAMATE COCAMIDOPROPYL BETAINE ERYTHRITOL BUTYLENE GLYCOL ALCOHOL HYDROXYACETOPHENONE 1,2-HEXANEDIOL PHENOXYETHANOL TOCOPHEROL SAURURUS CHINENSIS LEAF/ROOT EXTRACT TARAXACUM OFFICINALE (DANDELION) LEAF EXTRACT STEPHANIA TETRANDRA EXTRACT MENTHA HAPLOCALYX OIL CITRIC ACID PEG-40 HYDROGENATED CASTOR OIL

🎯 Purpose 1 words ▾

Astringent

📄 Keep Out of Reach of Children 16 words ▾

Keep out of reach of children lfswallowed,get medica help or contact aPoison Control Center right away.

📄 Package Label / Principal Display Panel 2 words ▾

label label2

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Hazel Perineal Healing Foam (this brand).

Top reported reactions

Erythema10
Skin Burning Sensation10
Nausea7
Dry Skin6
Fatigue6
Headache6
Acne5

Age at onset

Child1
Adult4
Elderly1

Reporter sex

87 reports
Male · 35%
Female · 65%

Serious outcomes

Disabling5
Life-threatening4
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 8 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Jiangsu Senwo Medical Technology 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 1 other package presentation of this same product, including 150 ml (85448-0001-02). 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?
Jiangsu Senwo Medical 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.
← 85447-0001-01 · Hiya 85448-0002-01 · Jiangsu →
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.