NDC 70082-0008-16 — Witch Hazel 86 g/100mL Liquid, 473 mL

🆔 Identity & classification

FDA NDC (as labeled) 70082-008-16

Product NDC 70082-008

11-digit billing NDC 70082000816

RxCUI 200295

UNII 101I4J0U34

UPC 0817415022271

Application # 505G(a)(3)

SPL Set ID a8eaa516-f830-410a-9f75-fa54903956cd

DEA schedule Non-controlled

Marketing category OTC MONOGRAPH DRUG

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2012-03-15

Route TOPICAL

Dosage form LIQUID

Substance WITCH HAZEL

Why two NDCs? The FDA registers this code as 70082-008-16 — 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 → 70082-0008-16. 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

LabelerDealMed Medical Supplies LLC

FDA application505G(a)(3) (OTC MONOGRAPH DRUG)

Labeler code70082

First marketedMar 2012

Product typeHuman Otc Drug

Portfolio3 products on file

🔎 All NDCs from DealMed Medical Supplies LLC

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?

Witch hazel is a liquid applied to the skin and is sold as an over-the-counter product under FDA's monograph rules for its category. The active ingredient, witch hazel extract, is commonly used in skincare products for its astringent properties, meaning it may help tighten or tone the skin. This product is typically used on minor skin irritations, minor cuts, or insect bites, though individual results may vary.

Patient education

📘 MedlinePlus patient leaflet ↗

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 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesAlcohol 14% by volume.

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 system	Per mL	Per 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Health Mart Witch Hazel 855 mg/mL 62011-0268-01	Strategic	473 ml	$0.006	—	FDA listed	—
Sunmark Witch Hazel 855 mg/mL 49348-0181-38	Strategic	473 ml	$0.007	—	Availability likely	—
GNP Witch Hazel 855 mg/mL 46122-0335-43	Amerisource	473 ml	$0.008	—	Availability likely	—
Witch Hazel 842 mg/mL 70000-0615-01	Cardinal	473 ml	$0.008	—	Availability likely	—
Witch Hazel 842 mg/mL 70677-1252-01	Strategic	473 ml	$0.008	—	Availability likely	—
Witch Hazel 860 mg/mL 00363-0803-43	Walgreen	473 ml	—	—	FDA listed	—
Witch Hazel 86 g/100mL 10565-0040-16	Hydrox	473 ml	—	—	FDA listed	—
Witch Hazel 86 g/100mL 10733-0801-08	Medical	236 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 11344-0822-43	Nice-Pak	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 21130-0822-43	Better	473 ml	—	—	FDA listed	—
Kroger Witch Hazel .86 g/mL 30142-0418-16	Kroger	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 30142-0822-43	The	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 37808-0822-43	H	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 41163-0822-43	United	473 ml	—	—	FDA listed	—
Witch Hazel 86 kg/100L 41250-0822-43	Meijer,	473 l	—	—	FDA listed	—
Witch Hazel 860 mg/mL 41520-0822-43	ADUSA	473 ml	—	—	FDA listed	—
Witch Hazel ReadyInCase 86 g/100mL 49580-0390-06	P	473 ml	—	—	FDA listed	—
TN Dickinsons Witch Hazel Astringent 86 g/100mL 52651-0001-04	Dickinson	3785 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 55301-0822-43	Your	473 l	—	—	FDA listed	—
Witch Hazel 860 mg/mL 56062-0822-43	Publix	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 59779-0045-43	CVS	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 63941-0822-43	Valu	473 ml	—	—	FDA listed	—
Witch Hazel 86 g/100mLthis 70082-0008-16	DealMed	473 ml	—	—	FDA listed	—
Witch Hazel 86 g/100mL 71990-0001-01	Arcadia	473 ml	—	—	FDA listed	—
Witch Hazel 860 mg/mL 72288-0922-26	Amazon.com	118 ml	—	—	Discontinued	—
Witch Hazel 860 mg/mL 76162-0822-43	Topco	473 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

🏛️

2012

On the market since

Mar 2012

📍

2026

Currently FDA-listed

14 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 Witch Hazel — the ingredient across all brands.

Top reported reactions

Haemorrhage27

Headache27

Rectal Haemorrhage27

Fatigue24

Nausea23

Diarrhoea22

Pain20

Age at onset

Infant1

Child1

Adolescent1

Adult11

Elderly7

Reporter sex

Male · 36%

Female · 64%

Unknown · 0%

Serious outcomes

Hospitalization96

Death19

Disabling13

Life-threatening10

Reports over time (by year) — tap or hover for the count & year

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 NDC	Description	Marketing start	Status
70082-0008-16 You're viewing this	473 mL in 1 BOTTLE, PLASTIC (70082-008-16)	2021-12-20	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 70082-008-16, 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: 70082-0008-16, written without dashes as 70082000816. 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 70082-0008-16, the first segment (70082) is the labeler code FDA assigned to DealMed Medical Supplies LLC; the middle segment (0008) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (16) 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 DealMed Medical Supplies LLC. Listing status can change — the directory data on this page refreshes weekly.

Who lists this product with the FDA?

DealMed Medical Supplies 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 13 words ▾

Uses: Relieves minor skin irritation due to: insect bites minor cuts minor scrapes

⏱️ Dosage and Administration 17 words ▾

Directions After cleansing apply generously to cotton ball and gently wipe skin. Apply as often as needed.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 5 words ▾

Active Ingredient Witch Hazel 86%

🧪 Inactive Ingredients 6 words ▾

Inactive ingredients Alcohol 14% by volume.

🎯 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 ↗

🔗 Related NDC lookups

🧪 All Witch Hazel NDCsSame ingredient 🏭 All DealMed labeler NDCsLabeler code 70082 📖 Read the Witch Hazel drug informationUses, warnings & side effects