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Soothing Hemorrhoidal Wipes 50 Witch Hazel 500 mg/mL Cloth, 30 patches — NDC 82637-0059-01 package photo

Soothing Hemorrhoidal Wipes 50 Witch Hazel 500 mg/mL Cloth, 30 patches

by The Honey Pot Company LLC · 30 PATCH in 1 POUCH (82637-0059-1) / 2.8 mL in 1 PATCH
NDC 82637-0059-01
🏷️ FDA NDC (as labeled) 82637-0059-1 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) 82637-0059-1
Product NDC 82637-0059
11-digit billing NDC 82637005901
RxCUI 844379
UNII 101I4J0U34
Application # M015
SPL Set ID 1ea202f5-e228-b3f2-e063-6294a90a16c1
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 TOPICAL
Dosage form CLOTH
Substance WITCH HAZEL
Why two NDCs? The FDA registers this code as 82637-0059-1 — 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 → 82637-0059-01. 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

LabelerThe Honey Pot Company LLC
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code82637
First marketedSep 2024
Product typeHuman Otc Drug
Portfolio4 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?

This is an over-the-counter topical wipe containing witch hazel, a plant extract commonly used as an astringent. Witch hazel is typically applied to the skin around the anal area to help reduce irritation and discomfort associated with hemorrhoids. The wipes come pre-moistened and ready to use on the affected area. This product is marketed under the FDA's monograph rules for over-the-counter hemorrhoidal treatments.

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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII 46AM2VJ0AW
    A dried fruit powder from the acai berry, used as a natural colorant and flavor ingredient to add purple-red color and fruity taste to medicines and supplements.
  • 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 ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII TRW2FUF47H
    A plant-derived powder from marshmallow root used as a binder and thickener in medicines. It helps hold ingredients together and can soothe irritated surfaces in throat lozenges and syrups.
  • UNII 0UE22Q87VC
    Apple cider vinegar is a sour liquid made from fermented apples. It's used in medicines as a flavoring agent and to help adjust the acidity level of the product.
  • UNII 5307V7XW8I
    A beneficial bacterium added to certain medicines and supplements. It acts as a probiotic ingredient, helping maintain or restore healthy gut bacteria balance in formulations designed for digestive wellness.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • 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 H2KVQ74JM4
    A compound derived from coconut oil that acts as a conditioning agent and surfactant. It helps stabilize and thicken liquid formulations while reducing static and improving texture in topical products.
  • UNII 3RT3536DHY
    A natural plant material derived from coconut that serves as a filler and texturizing agent in medicines. It helps give the product structure and consistency.
  • UNII YY7C30VXJT
    A natural plant extract from cucumber that adds flavor and freshness to medicines. It may also serve as a moisturizing agent or mild preservative in topical or oral formulations.
  • UNII 18L9G3U51M
    A gentle cleansing agent derived from coconut oil. It acts as a surfactant and emulsifier, helping mix oil and water-based ingredients together and improve how the product spreads or cleanses on skin.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • 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 Y9H1V576FH
    Honey is a natural sweetener made by bees from flower nectar. In medicines, it adds sweetness to improve taste and may help soothe throat irritation in lozenges or syrups.
  • UNII 2C1F12C6AP
    A beneficial live bacterium used as a probiotic ingredient. It's included to support the product's probiotic function by promoting beneficial microorganisms in the digestive system.
  • UNII Z6J799EAJK
    Oat is a cereal grain used in medicines as a filler and binder. It helps give the medication its shape and structure while adding bulk to the formulation.
  • 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 3N873UN885
    A plant-derived emulsifier made from glycerin and fatty acids. It helps blend oil and water-based ingredients together and improves how the medicine spreads or is absorbed.
  • UNII 56687D1Z4D
    A natural plant extract from pomegranate fruit, used as a flavor and color ingredient to enhance taste and appearance in medicines.
  • 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 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII B75E535IMI
    Sodium glycolate is a salt derived from glycolic acid, a naturally occurring compound. It works as a buffer and pH regulator in medicines, helping maintain the right acidity level for stability and absorption.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII 5EHL50I4MY
    A sodium salt compound used as a chelating agent in medicines. It binds to metals and minerals to improve stability, prevent discoloration, and help the medication stay effective longer.
  • 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.

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

The official label also stateswater, alcohol, aloe barbadensis leaf juice, cucumis sativus (cucumber) fruit extract, chamomilla recutita (matricaria) flower extract, calendula officinalis flower extract, althaea officinalis root extract, avena sativa (oat) kernel extract, cocos nucifera (coconut) fruit extract, apple cider vinegar, honey, helianthus annuus (sunflower) seed oil, euterpe oleracea fruit extract, lactobacillus, lactobacillus ferment, punica granatum fruit extract, tocopheryl acetate, polyglyceryl-4 caprate, propylene glycol, cocamidopropyl PG-dimonium chloride phosphate, glycerin, disodium cocoamphodiacetate, sodium chloride, sodium glycolate, sodium hydroxide, tetrasodium glutamate diacetate, citric acid, phenoxyethanol, ethylhexylglycerin, fragrance

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.
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 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/mLthis 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

🏛️
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.

🔬 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 Soothing Hemorrhoidal Wipes 50 Witch Hazel (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
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 6 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
82637-0059-01 You're viewing this 30 PATCH in 1 POUCH (82637-0059-1) / 2.8 mL in 1 PATCH 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 82637-0059-1, 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: 82637-0059-01, written without dashes as 82637005901. 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 82637-0059-01, the first segment (82637) is the labeler code FDA assigned to The Honey Pot Company LLC; the middle segment (0059) 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 The Honey Pot Company LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
The Honey Pot Company LLC 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 23 words ▾

Uses: Helps relieve the local itching and discomfort associated with hemorrhoids Temporary relief of irritation or burning Aids in protecting irritated anorectal areas

⏱️ Dosage and Administration 57 words ▾

Directions: Adults and children 12 years of age and older: Unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area Apply to the affected area up to 6 times daily or after each bowel movement Children under 12 years of age: Consult a doctor

⚠️ Warnings 86 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 doctor if: Bleeding occurs If symptoms persist for more than 7 days, or clear up and reoccur again within a few days. Keep out of reach of of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active Ingredient: Witch Hazel 50% Purpose: Astringent

🧪 Inactive Ingredients 83 words ▾

Inactive Ingredients: water, alcohol, aloe barbadensis leaf juice, cucumis sativus (cucumber) fruit extract, chamomilla recutita (matricaria) flower extract, calendula officinalis flower extract, althaea officinalis root extract, avena sativa (oat) kernel extract, cocos nucifera (coconut) fruit extract, apple cider vinegar, honey, helianthus annuus (sunflower) seed oil, euterpe oleracea fruit extract, lactobacillus, lactobacillus ferment, punica granatum fruit extract, tocopheryl acetate, polyglyceryl-4 caprate, propylene glycol, cocamidopropyl PG-dimonium chloride phosphate, glycerin, disodium cocoamphodiacetate, sodium chloride, sodium glycolate, sodium hydroxide, tetrasodium glutamate diacetate, citric acid, phenoxyethanol, ethylhexylglycerin, fragrance

🎯 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 ↗
← 82635-0403-01 · Melan 82637-9363-01 · The →
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.