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CVS Health Medicated WITCH HAZEL 500 mg Cloth — NDC 59779-0747-02 package photo

CVS Health Medicated WITCH HAZEL 500 mg Cloth

by CVS Pharmacy · 1 JAR in 1 CARTON (59779-747-02) / 100 CLOTH in 1 JAR
NDC 59779-0747-02
🏷️ FDA NDC (as labeled) 59779-747-02 billing pads the product segment with a zero
This package
Contains100 cloth in 1 jar Pack sizes5 compare ↓
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 →

🆔 Identity & classification

FDA NDC (as labeled) 59779-747-02
Product NDC 59779-747
11-digit billing NDC 59779074702
NCPDP billing unit EA — each (per item)
RxCUI 844379
UNII 101I4J0U34
Application # M016
SPL Set ID a74ab253-cafc-4f00-9b8f-e5c1e6e7f221
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-11-24
Route TOPICAL
Dosage form CLOTH
Substance WITCH HAZEL
GPI-14 90970035004300
GPI class CVS Medicated Witch Hazel
GCN Seq No 066102
GCN 28286
HICL code 021836
Ingredient (HICL) Witch Hazel
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q3
Therapeutic class — intermediate (HIC2) Anal-Rectal Preparations
HIC3 code Q3D
Therapeutic class — specific (HIC3) Hemorrhoidal Preparations
AHFS code 84:12.00.00
AHFS class Astringents (84:12)
FDB label name CVS MEDICATED 50% PADS
FDB brand name Medicated Pads
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 59779-747-02 — 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 → 59779-0747-02. 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

LabelerCVS Pharmacy
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code59779
First marketedNov 2015
Product typeHuman Otc Drug
Portfolio550 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

Label name CVS MEDICATED 50% PADS Ingredient Witch Hazel
🧪 What is this product?

This product is a medicated cloth containing witch hazel, an herbal extract typically used as a topical astringent and skin soother. It is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rules for this category of products rather than being individually reviewed. The cloth form is designed for convenient topical application to skin. Witch hazel is commonly used in products meant to temporarily tighten and refresh the skin.

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 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 V5VD430YW9
    A plant-derived substance from the aloe vera leaf. Used in medicines as a natural flavor, skin-soothing agent in topical products, and sometimes as a mild laxative ingredient in oral formulations.
  • 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 Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • 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 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • 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.

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

The official label also statesWater, Alcohol, Glycerin, Phenoxyethanol, Aloe, Decyl Glucoside, Potassium Sorbate, Propylene Glycol, Sodium Benzoate, Citric Acid.

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 DailyMedingredient 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: 1 jar 10 cloths 48 cloths 96 cloths
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
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/1000mg 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 mgthis 59779-0747-02 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

🏛️
2015
On the market since
Nov 2015
📍
2026
Currently FDA-listed
11 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.

🔬 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 CVS Health Medicated (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
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
59779-0747-01 1 JAR in 1 CARTON (59779-747-01) / 50 CLOTH in 1 JAR 2015-11-24 Active
59779-0747-02 You're viewing this 1 JAR in 1 CARTON (59779-747-02) / 100 CLOTH in 1 JAR 2015-11-24 Active
59779-0747-10 1 PACKAGE in 1 CARTON (59779-747-10) / 10 CLOTH in 1 PACKAGE 2022-06-30 Active
59779-0747-48 1 CARTON in 1 CARTON (59779-747-48) / 48 CLOTH in 1 CARTON 2021-07-07 Active
59779-0747-96 1 PACKAGE in 1 CARTON (59779-747-96) / 96 CLOTH in 1 PACKAGE 2022-06-30 Active

Pack size FAQ

What quantity is in NDC 59779-0747-02?
NDC 59779-0747-02 is listed by the FDA — 1 jar in 1 carton / 100 cloth in 1 jar.
What NDC number is used to bill for this package of CVS Health Medicated WITCH HAZEL 500 mg Cloth?
Bill NDC 59779-0747-02 — the 11-digit billing format is 59779074702. 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
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 59779-747-02, 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: 59779-0747-02, written without dashes as 59779074702. 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 59779-0747-02, the first segment (59779) is the labeler code FDA assigned to CVS Pharmacy; the middle segment (0747) 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.
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 CVS Pharmacy. 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 4 other package presentations of this same product, including 1 jar (59779-0747-01), 10 cloths (59779-0747-10), 48 cloths (59779-0747-48). 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?
CVS Pharmacy 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 23 words

Uses helps relieve the local itching and discomfort associated with hemorrhoids temporary relief of irritation and burning. aids in protecting irritated anorectal areas.

⏱️ Dosage and Administration 62 words

Directions adult: cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area. use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discard children under 12 years of age: consult a doctor do not flush in toilets, dispose of pad in trash after use.

⚠️ Warnings 85 words

Warnings For external use only. When using this product do not exceed the recommended daily dosage unless directed by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if bleeding occurs condition worsens or does not improve within 7 days Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away. (1-800-222-1222). If pregnant or breast-feeding, ask a health professional before use.

🧪 Active Ingredient 5 words

Active ingredient Witch hazel 50%

🧪 Inactive Ingredients 17 words

Inactive ingredients Water, Alcohol, Glycerin, Phenoxyethanol, Aloe, Decyl Glucoside, Potassium Sorbate, Propylene Glycol, Sodium Benzoate, Citric Acid.

🎯 Purpose 2 words

Purpose Astringent

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