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medicated wipes Witch Hazel 500 mg/1000mg Patch — NDC 41250-0988-48 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

medicated wipes Witch Hazel 500 mg/1000mg Patch — NDC 41250-988-48 (Billing 41250-0988-48)

by Meijer Distribution Inc. · 48 PATCH in 1 BOX / 500 mg in 1 PATCH

This is a package of medicated wipes Witch Hazel 500 mg/1000mg Patch from Meijer Distribution Inc., marketed since Jun 2018 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 41250-0988-48
🏷️ FDA NDC (as labeled) 41250-988-48 billing pads the product segment with a zero
This package
Contains500 mg in 1 patch Pack sizes2 compare ↓
Main listing for product 41250-988 · Also comes in: 96 patches 41250-988-96
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 41250-988-48 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41250 labeler · 988 product · 48 package
Package marketed since
Oct 2, 2019
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 4125098848 0
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41250-988-48
Product NDC 41250-988
11-digit billing NDC 41250098848
RxCUI 844379
UNII 101I4J0U34
Application # M015
SPL Set ID ba0f3f9a-95d1-4d8a-86d1-2c25c945118c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-06-28
Route TOPICAL
Dosage form PATCH
Substance WITCH HAZEL
Quick answers
  • RxCUI (RxNorm): 844379
Why two NDCs? The FDA registers this code as 41250-988-48 — 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 → 41250-0988-48. 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 an over-the-counter topical patch containing witch hazel, an herbal extract commonly used in skin care products. Witch hazel is typically applied to skin to help soothe minor irritation and reduce puffiness. This product is marketed under the FDA's OTC monograph rules for its category rather than through an individual drug application. The patch form allows for localized, hands-free delivery of the ingredient to affected areas.

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 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: 96 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
41250-0988-48 You're viewing this Main listing 48 PATCH in 1 BOX / 500 mg in 1 PATCH 2019-10-02 — Active
41250-0988-96 41250-988-96 96 PATCH in 1 BAG / 500 mg in 1 PATCH 2019-10-02 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 48 patch in 1 box / 500 mg in 1 patch.
What NDC number is used to bill for this package of medicated wipes Witch Hazel 500 mg/1000mg Patch?
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
Major Medi-Pads 50 g/100g 00904-6829-60 Major 100 packets $0.044 — Availability likely —
Medicated Hemorrhoidal Pads 500 mg/mL 70000-0364-01 Cardinal 1 jar $0.044 — Availability likely —
QC Medicated Cooling 500 mg 83324-0311-01 Chain 1 jar $0.044 — Availability likely —
Pre-moistened Medicated Wipes, Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent, Walgreens Pre-moistened Medicated Wipes, Walgreens Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent 50 mg/100mg 00363-1740-48 Walgreens 48 patches — — FDA listed —
Preparation H Medicated Wipes 5 g 00573-0556-07 Haleon 10 packets — — FDA listed —
Preparation H Medicated Wipes 5 g 00573-0557-01 Haleon 48 cloths — — FDA listed —
Preparation H Totables Irritation Relief Wipes 5 g 00573-0558-07 Haleon 10 packets — — FDA listed —
Tucks Medicated Cooling Pads 500 mg/mL 10157-2103-01 Blistex 1 jar — — FDA listed —
up and up medicated wipes manixim strength .5 g/g 11673-0404-48 Target 48 applicators — — FDA listed —
medicated pads 50 mg/100mg 11673-0614-10 TARGET 100 patches — — FDA listed —
Signature Care Medicated Wipes Hemorrhoidal Wipes with Witch Hazel .5 mg/mL 21130-0800-48 Better 252 ml — — FDA listed —
Signature Care Medicated Cooling 500 mg 21130-0928-00 Better 100 cloths — — FDA listed —
Kroger Medicated Wipes Hemorrhoidal Wipe With Witch Hazel And Aloe .5 g/g 30142-0791-71 The 252 g — — FDA listed —
hemorrhoidal pads 500 mg/1000mg 41250-0868-10 Meijer 100 patches — — FDA listed —
medicated wipes 500 mg/1000mgthis 41250-0988-48 Meijer 48 patches — — FDA listed —
Maximum Strength Hemorrhoidal Pads 500 mg 49035-0465-10 Walmart, 100 cloths — — FDA listed —
Equate Hemorrhoidal Medicated Wipes .5 mg/mL 49035-0793-41 Walmart 252 ml — — FDA listed —
AER Pre-moistened Witch Hazel Pad 500 mg/mL 50289-3250-01 Birchwood 40 applicators — — FDA listed —
AER Traveler Towelette .5 g 50289-4200-01 Birchwood 50 packets — — FDA listed —
B-SURE Traveler Towelette .5 g/g 50289-9250-01 Birchwood 4 g — — FDA listed —
Good Sense Medicated 500 mg 50804-0047-60 Geiss, 100 cloths — — FDA listed —
GOODSENSE Maximum Strength Medicated 50 g/100g 50804-0211-48 GEISS, 48 packets — — FDA listed —
Perineal Cooling Liners 500 mg/g 51316-0716-00 CVS 24 patches — — FDA listed —
TN Dickinsons Witch Hazel Hemorrhoidal Pads 1.2 g 52651-0003-01 Dickinson 1 jar — — FDA listed —
T.N. Dickinsons Witch Hazel Medicated Cooling Pads Hemorrhoidal Relief .034 g 52651-0010-01 Dickinson 1 jar — — FDA listed —
The Pharma-C Company Medicated Hemorrhoidal Pads 500 mg/mL 55239-0359-00 Kleen 100 patches — — FDA listed —
Medicated Wipes Hemorroidal Wipes With Witch Hazel 500 mg/mL 55319-0402-00 FAMILY 48 patches — — Discontinued —
FAMILY Wellness MEDICATED HEMORRHOIDAL WIPES 50 g/100mL 55319-0774-01 Family 1 pouch — — FDA listed —
Rexall Medicated WipesHemorrhoidal wipe Hemorrhoidal wipes with witch hazel 129 g/258g 55910-0105-48 Old 258 g — — FDA listed —
Witch Hazel 50 g/1001 56194-0550-01 Giant 48 cloths — — FDA listed —
Geri Care Medicated Pads 50 mg/mL 57896-0115-01 Geri-Care 100 patches — — FDA listed —
Medicated Wipes Hemorrhoidal Wipes with Witch Hazel .5 g/g 59779-0607-10 CVS 48 applicators — — FDA listed —
CVS Health Medicated 500 mg 59779-0747-01 CVS 1 jar — — FDA listed —
Meicated Wipe 50 g/100g 64709-0120-01 Diamond 195.09 g — — FDA listed —
Dr Talbots Cooling Perineal Pad .5 g/g 70797-0104-01 Talbot's 120 g — — FDA listed —
Dr Butlers Hemorrhoid 50 g/100g 70942-0100-48 Beyond 3 g — — FDA listed —
Hemorrhoidal Hygiene pads 50 g/100mL 71399-0110-01 Akron 175 ml — — FDA listed —
Flushable Hemorrhoidal Medicated Wipes Maximum Strength .5 g 72288-0923-01 Amazon.com 48 cloths — — FDA listed —
frida mom Perineal Cooling Pad Liners .5 g 72705-0100-01 Fridababy, 24 cloths — — FDA listed —
Perineal Cooling Pad Liners 50 g/100g 72705-0420-01 Fridababy, 100 g — — FDA listed —
Medicated Wipes Hemorroidal Wipes With Witch Hazel 500 mg/mL 72932-0009-00 Wuhan 48 patches — — FDA listed —
Medicated Multipurpose Wipes 50 mg/100mg 78691-0050-15 QUEST 15 patches — — FDA listed —
Soothing Hemorrhoidal Wipes 50 Witch Hazel 500 mg/mL 82637-0059-01 The 30 patches — — FDA listed —
Pura 50 mg 84217-0050-48 Mypura.com 48 patches — — FDA listed —
Norms Medicated Wipes .5 g/g 85996-0001-01 Totally 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

🏛️
2018
On the market since
Jun 2018
📍
2026
Currently FDA-listed
8 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 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 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.
  • 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 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • 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.

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

The official label also statesWater, Sodium citrate, Citric acid, Glycerin, Phenoxyethanol, Potassium sorbate

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

LabelerMeijer Distribution Inc.
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code41250
First marketedJun 2018
Product typeHuman Otc Drug
Portfolio37 products on file

More NDCs from Meijer Distribution Inc. labeler code 41250

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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

Uses Temporarily relieves these external symptoms associated with hemorrhoids: itching burning irritation

⏱️ Dosage and Administration 68 words ▾

Directions As hemorrhoidal treatment for adults: when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. gently dry by patting or blotting with toilet tissue or soft cloth before applying. gently apply to the affected area by patting and then discard. can be used up to six times daily or after each bowel movement. Children under 12 years of age consult a doctor.

⚠️ Warnings 74 words ▾

Warnings For external rectal use only. When using this product do not exceed the recommended daily dosage unless directed by a doctor. do not insert into rectum or vagina using fingers or mechanical device. Stop use and ask a doctor if rectal bleeding occurs condition worsens or does not improve within 7 days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

📦 Storage and Handling 9 words ▾

Other Information Store at controlled room temperature: 15º-30ºC (59º-86ºF)

🧪 Active Ingredient 5 words ▾

Active Ingredient Witch Hazel 50%

🧪 Inactive Ingredients 11 words ▾

Inactive Ingredients Water, Sodium citrate, Citric acid, Glycerin, Phenoxyethanol, Potassium sorbate

🎯 Purpose 3 words ▾

Purpose Hemorrhoidal Astringent

📄 Ask a Doctor Before Use If 19 words ▾

Stop use and ask a doctor if rectal bleeding occurs condition worsens or does not improve within 7 days.

📄 When Using This Product 28 words ▾

When using this product do not exceed the recommended daily dosage unless directed by a doctor. do not insert into rectum or vagina using fingers or mechanical device.

📄 Keep Out of Reach of Children 21 words ▾

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

📄 Package Label / Principal Display Panel 97 words ▾

Principal Display Panel NDC 41250-988-48 meijer Compare to Preparation H® active ingredient* medicated wipes Hemorrhoidal Wipes with Witch Hazel MAXIMUM STRENGTH Provides Temporary Relief of Itching, Burning and Irritation 48 WIPES 6 IN x 5 IN (15cm x 12cm) NDC 41250-988-96 meijer Compare to Preparation H® active ingredient* medicated wipes Hemorrhoidal Wipes with Witch Hazel MAXIMUM STRENGTH Provides Temporary Relief of Itching, Burning and Irritation For Use with Hemorrhoids and for Vaginal Care Convenient, Easy to Use 96 WIPES (2 x 48 CT.

PACKS) 6 IN x 5 IN (15.2 cm x 12.7 cm) 48 49 96

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 medicated wipes (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

Hospitalization28
Death7
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 Meijer Distribution Inc.. 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 96 patches (41250-0988-96). 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?
Meijer Distribution Inc. 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.
← 41250-0986-22 · Meijer 41250-0989-10 · Meijer →
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.