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Humphreys Maravilla witch hazel 1 g/mL Liquid, 237 mL — NDC 00219-0204-80 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Humphreys Maravilla witch hazel 1 g/mL Liquid, 237 mL — NDC 0219-0204-80 (Billing 00219-0204-80)

by Humphreys Pharmacal, Incorporated · 237 mL in 1 BOTTLE, PLASTIC

This is a package of 237 mL of Humphreys Maravilla witch hazel 1 g/mL Liquid from Humphreys Pharmacal, Incorporated, marketed since Jan 1955 and currently FDA-listed.

NDC 00219-0204-80
🏷️ FDA NDC (as labeled) 0219-0204-80 billing pads the labeler segment with a zero
This package
Contains237 mL Pack sizes2 compare ↓
Product page 00219-0204-16 Also comes in: 473 ml 0219-0204-16
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 0219-0204-80 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0219 labeler · 0204 product · 80 package
Package marketed since
Jan 11, 1955
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0302190204160
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0219-0204-80
Product NDC 0219-0204
11-digit billing NDC 00219020480
UNII 101I4J0U34
UPC 0302190204160
Application # M016
SPL Set ID 7d403bf4-8a0d-4337-8e81-1149cd0ae1dc
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1955-01-11
Route TOPICAL
Dosage form LIQUID
Substance WITCH HAZEL

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 005690
GCN 22610
HICL code 002425
Ingredient (HICL) Witch Hazel Leaf
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L4
Therapeutic class — intermediate (HIC2) Astringents
HIC3 code L4A
Therapeutic class — specific (HIC3) Astringents
AHFS code 84:12.00.00
AHFS class Astringents (84:12)
FDB label name HUMPHREYS WITCH HAZEL LIQ
FDB brand name Humphreys Witch Hazel
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 005690
  • GCN: 22610
  • HICL (First Databank): 002425
  • AHFS class code: 84:12.00.00
Why two NDCs? The FDA registers this code as 0219-0204-80 — a 4-4-2 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 labeler segment → 00219-0204-80. 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

Label name HUMPHREYS WITCH HAZEL LIQ Ingredient Witch Hazel Leaf
🧪 What is this product?

Humphreys Maravilla witch hazel is a topical liquid containing witch hazel extract. This product is marketed as an over-the-counter monograph drug, meaning it is sold under FDA's established rules for this category of product. Witch hazel is commonly used as an astringent in topical preparations, typically applied to skin for cleansing and toning purposes.

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 mLPer 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: 473 ml
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
00219-0204-16 0219-0204-16 Main listing 473 mL in 1 BOTTLE, PLASTIC 1955-01-11 — Active
00219-0204-80 You're viewing this 237 mL in 1 BOTTLE, PLASTIC 1955-01-11 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 237 mL — 237 ml in 1 bottle, plastic.
How does this package differ from NDC 00219-0204-16?
Both are Humphreys Maravilla witch hazel 1 g/mL Liquid — the drug itself is identical. This page's package is the 237 mL one, while NDC 00219-0204-16 is the 473 ml package.
What NDC number is used to bill for this package of Humphreys Maravilla witch hazel 1 g/mL Liquid?
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
Humphreys Maravilla 1 g/mLthis 00219-0204-80 Humphreys 237 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

🏛️
1955
On the market since
Jan 1955
📍
2026
Currently FDA-listed
71 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.

A current SPL was checked, but it does not contain a structured or narrative inactive-ingredient list for this product. This does not mean the product has no inactive ingredients.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerHumphreys Pharmacal, Incorporated
FDA applicationM016 (OTC MONOGRAPH DRUG)
Labeler code00219
First marketedJan 1955
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.

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 🎯 Purpose 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 29 words ▾

Usos/Uses: Alivia temporalmente irritaciones de la piel debido a: cortadas menores raspaduras menores picaduras de insectos Temporarily relieves minor skin irritations due to: minor cuts minor scrapes insect bites

⏱️ Dosage and Administration 43 words ▾

Instrucciones/Directions: Remueva el sello interno / Remove protective inner seal Humedezca un algodón o almohadilla y limpie suavemente la piel / Moisten cotton ball or cleansing pad and gently wipe skin. Aplique las veces que sea necesario / Apply as often as necessary

⚠️ Warnings 31 words ▾

Advertencias / Warnings: Para uso externo solamente / For external use only. Cuando use este producto evite el contacto con los ojos / When using this product avoid contact with eyes.

📦 Storage and Handling 14 words ▾

Otra información / Other information Almacenar por debajo de 30C / Store below 86F

🧪 Active Ingredient 16 words ▾

Hamamelis Virginiana (witch hazel) destilada 86%, Alcohol 14% Hamamelis Virginiana (witch hazel) distillate 86%, Alcohol 14%

🎯 Purpose 3 words ▾

Propósito/Purpose Astringente Astringent

📄 Stop Use and Ask a Doctor If 36 words ▾

Si los síntomas empeoran o persisten por más de 7 días, suspenda su uso y consulte a su médico / Stop use and ask doctor if condition worsens or symptoms persist for more than 7 days.

📄 Keep Out of Reach of Children 30 words ▾

Mantenga alejado de los niños. Si se ingiere busque ayuda médica inmediatamente Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

📄 Questions or Comments 16 words ▾

Distribuido por / Dist. by: Humphreys Pharmacal, Inc. East Hampton, CT 06424 Made in USA www.humphreysusa.com

📄 Package Label / Principal Display Panel 38 words ▾

Product Packaging The labels shown below represent a sample of that currently in use. Additional packaging may also be available. HUMPHREYS MARAVILLA LOTION 100% All Natural Witch Hazel since 1854 ASTRINGENTE - CALMANTE - REFRESCANTE Maravilla FB Labels

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

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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Humphreys Pharmacal, Incorporated. 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 473 ml (00219-0204-16). 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?
Humphreys Pharmacal, Incorporated 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.
← 00206-8862-02 · Wyeth 00220-0002-41 · BOIRON →
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.