Witch Hazel 860 mg/mL Liquid, 236 mL
by H E B · 236 mL in 1 BOTTLE, PUMP (37808-822-99)
NDC 37808-0822-99
🏷️ FDA NDC (as labeled)
37808-822-99
billing pads the product segment with a zero
This package
Contains236 mL
Pack sizes3 compare ↓
OTC
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ 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 →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
37808-822-99
Product NDC
37808-822
11-digit billing NDC
37808082299
RxCUI
200295
UNII
101I4J0U34
Application #
M015
SPL Set ID
09b814f4-86b5-4810-bf52-cc88396451c2
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2015-06-18
Route
TOPICAL
Dosage form
LIQUID
Substance
WITCH HAZEL
Why two NDCs?
The FDA registers this code as 37808-822-99 — 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 → 37808-0822-99. 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
LabelerH E B
FDA applicationM015 (OTC MONOGRAPH DRUG)
Labeler code37808
First marketedJun 2015
Product typeHuman Otc Drug
Portfolio264 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 a topical liquid product containing witch hazel, an herbal extract commonly applied to the skin. Witch hazel is traditionally used in over-the-counter products for cleansing and as an astringent, meaning it is thought to help tighten or tone the skin. This product is marketed as an OTC monograph drug, which means it follows established FDA guidelines for this category rather than undergoing individual new drug review. The liquid form allows for easy application directly to the skin.
Patient education
Supplement & herbal interactions
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.
💬 Questions about Witch Hazel?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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 statesNone
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
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/mLthis 37808-0822-99 | H | 236 ml | — | — | Discontinued | — |
| 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/100mL 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
🏛️
2015
On the market since
Jun 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 Witch Hazel — the ingredient across all brands.
Top reported reactions
Age at onset
Reporter sex
Male · 36%
Female · 64%
Unknown · 0%
Serious outcomes
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 |
|---|---|---|---|
| 37808-0822-43 | 473 mL in 1 BOTTLE, PLASTIC (37808-822-43) | 2015-06-18 | Active |
| 37808-0822-45 | 946 mL in 1 BOTTLE, PLASTIC (37808-822-45) | 2015-06-18 | Discontinued by firm |
| 37808-0822-99 You're viewing this | 236 mL in 1 BOTTLE, PUMP (37808-822-99) | 2015-06-18 | Discontinued by firm |
You're viewing the smallest of 3 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 37808-0822-99?
NDC 37808-0822-99 contains 236 mL — 236 ml in 1 bottle, pump.
What is the difference between NDC 37808-0822-99 and NDC 37808-0822-43?
Both are Witch Hazel 860 mg/mL Liquid — the drug itself is identical. NDC 37808-0822-99 is the 236 mL package, while NDC 37808-0822-43 is the 473 ml package.
What NDC number is used to bill for this package of Witch Hazel 860 mg/mL Liquid?
Bill NDC 37808-0822-99 — the 11-digit billing format is 37808082299. 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
No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 37808-822-99, 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: 37808-0822-99, written without dashes as 37808082299. 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 37808-0822-99, the first segment (37808) is the labeler code FDA assigned to H E B; the middle segment (0822) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (99) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 473 ml (37808-0822-43), 946 ml (37808-0822-45). 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?
H E B 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
🤒 Adverse Reactions
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Use for relief of minor skin irritations due to: insect bites minor cuts minor scrapes
⏱️ Dosage and Administration ▾
Directions apply as often as needed
⚠️ Warnings ▾
Warnings For external use only
🤒 Adverse Reactions ▾
adverse reaction MADE WITH PRIDE & CARE FOR H-E-B ® SAN ANTONIO, TX 78204 100% GUARANTEE promise If you aren't completely pleased with this product, we'll be happy to replace it or refund your money. You have our word on it. Pat. D675, 101
🧪 Active Ingredient ▾
Active ingredient Witch hazel 100% (containing alcohol 14% by volume)
🧪 Inactive Ingredients ▾
Inactive ingredient None
🎯 Purpose ▾
Purpose Astringent
No label section mentions that — try another word, or open the full label on DailyMed below.
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.