Home › NDC Lookup › Ingredients › Witch Hazel, Pleione, Aloe, Mint › 85511-0001-02
WOWDAY MEDICATED HEMORRHOIDAL FLUSHABLE WIPES Witch Hazel, Pleione, Aloe, Mint 10 mg/100mg; 8 mg/100mg; 20 mg/100mg; 20 mg/100mg Patch — NDC 85511-0001-02 package photo

WOWDAY MEDICATED HEMORRHOIDAL FLUSHABLE WIPES Witch Hazel, Pleione, Aloe, Mint 10 mg/100mg; 8 mg/100mg; 20 mg/100mg; 20 mg/100mg Patch

by Shanghai Tongjie Commodity Co.,Ltd. · 12 PATCH in 1 BAG (85511-001-02) / 100 mg in 1 PATCH
NDC 85511-0001-02
🏷️ FDA NDC (as labeled) 85511-001-02 billing pads the product segment with a zero
This package
Contains100 mg in 1 patch Pack sizes2 compare ↓
Also comes in: 56 patches 85511-0001-01
OTC Discontinued Non-controlled ⚠ Inactivated by FDA
🗂️ 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

⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 85511-001-02
Product NDC 85511-001
11-digit billing NDC 85511000102
UNII 101I4J0U34, FV98Z8GITP, V5VD430YW9, 7DX1GAG1PE
Application # 505G(a)(3)
SPL Set ID 325b2637-ec39-fc14-e063-6394a90a1e23
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2025-04-09
Route TOPICAL
Dosage form PATCH
Substance WITCH HAZEL; MINT; ALOE; PLEIONE YUNNANENSIS WHOLE
Why two NDCs? The FDA registers this code as 85511-001-02 — 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 → 85511-0001-02. 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

LabelerShanghai Tongjie Commodity Co.,Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85511
First marketedApr 2025
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 a topical medicated wipe product marketed as an over-the-counter monograph drug. It contains witch hazel, aloe, mint, and pleione yunnanensis, ingredients typically used in hemorrhoidal care products for their soothing and astringent properties. Witch hazel and pleione are commonly included for their astringent effects, while aloe and mint are typically added for their cooling and soothing sensations. The wipes are designed for topical application to the affected area.

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 C8IYT9CR7C
    Aloe emodin is a yellow compound derived from aloe plants. In medicines, it may function as a coloring agent or contribute to the formulation's stability and appearance.
  • UNII PQ6CK8PD0R
    Ascorbic acid, also known as vitamin C, is a white crystalline powder. It serves as an antioxidant to prevent degradation of other ingredients and may also function as a preservative in the formulation.
  • UNII 4313O7P4XW
    Cholesteryl nonanoate is a cholesterol derivative used as a penetration enhancer and emollient in topical formulations. It helps active ingredients absorb through the skin and improves the texture and feel of creams and ointments.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII SML2Y3J35T
    Colchicine is an alkaloid compound derived from the autumn crocus plant. In medications, it acts as the active therapeutic ingredient rather than an inactive excipient, so it would not typically appear listed as a separate excipient on a drug label.
  • UNII 36W3E5TAMG
    Glucomannan is a natural soluble fiber derived from the konjac plant. In medications, it acts as a binder and bulking agent, helping hold ingredients together and add volume to the formulation.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • UNII Z46B1LUI5N
    Mimosine is a naturally occurring amino acid compound extracted from legume plants. In medications, it serves as a buffering or pH-adjusting agent to help stabilize the formulation and maintain proper acidity levels.
  • UNII TF9HZN9T0M
    Pinitol is a naturally occurring sugar alcohol derived from plants. In medicines, it functions as a sweetener and may help improve tablet texture and stability during storage.
  • UNII B3FUD0528F
    Rebaudioside A is a naturally derived sweetener extracted from stevia leaves. It sweetens the medicine without adding calories and helps mask bitter tastes to improve how the medication goes down.
  • UNII 81G40H8B0T
    Vitamin A is a fat-soluble nutrient that acts as a colorant and antioxidant in medications. It prevents oxidation of other ingredients and may add nutritional value to the formulation.
  • UNII O03S90U1F2
    A synthetic compound combining vitamin E with polyethylene glycol and succinic acid. It acts as a solubilizer and antioxidant in medicines, helping dissolve poorly water-soluble drugs and prevent degradation of active 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesVitamin A Vitamin C Vitamin E Glycyrrhizic acid Mimosine D-Pinitol Colchicine Aloe-emodin glycoside Polysaccharide Citric acid Glycoside Cholesterin Menthol Glucomannan Purified water

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 eachPer 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: 56 patches
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
Wowday Medicated Hemorrhoidal Flushable Wipes 10 mg/100mg; 8 mg/100mg; 20 mg/100mg; 20 mg/100mgthis 85511-0001-02 Shanghai 12 patches — — Discontinued —
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
Apr 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
85511-0001-01 56 PATCH in 1 BAG (85511-001-01) / 100 mg in 1 PATCH 2025-04-09 Inactivated by FDA
85511-0001-02 You're viewing this 12 PATCH in 1 BAG (85511-001-02) / 100 mg in 1 PATCH 2025-04-09 Inactivated by FDA

Pack size FAQ

What quantity is in NDC 85511-0001-02?
NDC 85511-0001-02 is listed by the FDA — 12 patch in 1 bag / 100 mg in 1 patch.
What NDC number is used to bill for this package of WOWDAY MEDICATED HEMORRHOIDAL FLUSHABLE WIPES Witch Hazel, Pleione, Aloe, Mint 10 mg/100mg; 8 mg/100mg; 20 mg/100mg; 20 mg/100mg Patch?
Bill NDC 85511-0001-02 — the 11-digit billing format is 85511000102. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 85511-001-02, 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: 85511-0001-02, written without dashes as 85511000102. 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 85511-0001-02, the first segment (85511) is the labeler code FDA assigned to Shanghai Tongjie Commodity Co.,Ltd.; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 56 patches (85511-0001-01). 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?
Shanghai Tongjie Commodity 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 93 words ▾

0pen the lid on the top of the wipes pouch Peel back wipes seal, remove completely and discard Grab the top wipe at the edge of the center fold and pull out of pouch Close lid after each use to retain moisture Adults: Unfold wipe and cleanse the area by gently wiping, pating or blotting. lf necessary, repeat until all matter is removed from the area.Use up to 6 times daily or after each bowel movement and before applying topical hemorrhoidal treatments and then discardChildren under 12 years of age: consult a doctor

⏱️ Dosage and Administration 45 words ▾

Adults: Unfold wipe and cleanse the area by gently wiping, pating or blotting. lf necessary, repeat unti all matter is removed from the area. I Use up to 6 times daily or after each bowel movement and before applying topical hemorrhoidal treatments and then discard

⚠️ Warnings 4 words ▾

For external use only

🧪 Active Ingredient 5 words ▾

Witch Hazel, Pleione, Aloe, Mint

🧪 Inactive Ingredients 22 words ▾

Vitamin A Vitamin C Vitamin E Glycyrrhizic acid Mimosine D-Pinitol Colchicine Aloe-emodin glycoside Polysaccharide Citric acid Glycoside Cholesterin Menthol Glucomannan Purified water

🎯 Purpose 8 words ▾

EVERYDAY CLEANSING & SOOTHINGI SAFE FOR INTIMATE USE

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85510-0101-01 · RoseWell 85512-1028-01 · Qingdao →
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.