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DHS tar gel coal .005 g/g Shampoo, 20.8 g — NDC 00096-0736-22 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

DHS tar gel coal .005 g/g Shampoo, 20.8 g — NDC 0096-0736-22 (Billing 00096-0736-22)

by Person and Covey · 20.8 g in 1 BOTTLE

This is a package of 20.8 g of DHS tar gel coal .005 g/g Shampoo from Person and Covey, marketed since Jun 1996 and currently FDA-listed.

NDC 00096-0736-22
🏷️ FDA NDC (as labeled) 0096-0736-22 billing pads the labeler segment with a zero
This package
Contains20.8 g Pack sizes2 compare ↓
Product page 00096-0736-08 Also comes in: 249.6 g 0096-0736-08
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0096-0736-22
Product NDC 0096-0736
11-digit billing NDC 00096073622
RxCUI 210490, 309381
UNII R533ESO2EC
Application # M032
SPL Set ID e17bd664-748b-417c-a247-9acc7bc7eec3
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1996-06-01
Route TOPICAL
Dosage form SHAMPOO
Substance COAL TAR

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

GPI-14 90520010004505
GPI class DHS Tar Gel
GCN Seq No 005977
GCN 23611
HICL code 002557
Ingredient (HICL) Coal Tar
HIC1 code L
Therapeutic class — broad (HIC1) Skin/Subcutaneous Tissue
HIC2 code L6
Therapeutic class — intermediate (HIC2) Irritants
HIC3 code L6A
Therapeutic class — specific (HIC3) Irritants/Counter-Irritants
AHFS code 84:32.00.00
AHFS class Keratoplastic Agents
FDB label name DHS TAR GEL 0.5% SHAMPOO
FDB brand name Dhs Tar Gel
Legend status O — Over-the-counter (OTC) drug or device
Quick answers
  • GSN (GCN sequence number): 005977
  • GCN: 23611
  • GPI-14 (Medi-Span): 90520010004505
  • HICL (First Databank): 002557
  • AHFS class code: 84:32.00.00
  • RxCUI (RxNorm): 210490
Why two NDCs? The FDA registers this code as 0096-0736-22 — 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 → 00096-0736-22. 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 DHS TAR GEL 0.5% SHAMPOO Ingredient Coal Tar
📗 Our plain-language guide HelloPharmacist
  • It relieves the itching, scaling, flaking and redness of psoriasis, seborrheic dermatitis and dandruff. Which of these a product treats depends on the brand, so check your package....
  • It depends on the product. Most coal tar shampoos say to use them at least twice a week, leaving the lather on for several minutes. Some ointments, gels and lotions can be used one...
  • Be careful. Coal tar can make you more likely to sunburn for up to 24 hours after you apply it. Cover up and limit sun exposure during that time.
  • Don't combine it with light therapy or prescription psoriasis medicines unless your doctor says it's okay. Check with me or your doctor first if you're not sure.
📖 Read our full Coal Tar guide →

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 gPer 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: 249.6 g
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 Per unit Per pack Marketing startMarketing endStatus
00096-0736-08 0096-0736-08 Main listing 249.6 g in 1 BOTTLE $0.0411 / mL — 1996-06-01 — Active
00096-0736-22 You're viewing this 20.8 g in 1 BOTTLE Sample — — 2026-03-04 — Active

Pack size FAQ

What quantity is in this package?
This package contains 20.8 g — 20.8 g in 1 bottle.
How does this package differ from NDC 00096-0736-08?
Both are DHS tar gel coal .005 g/g Shampoo — the drug itself is identical. This page's package is the 20.8 g one, while NDC 00096-0736-08 is the 249.6 g package.
What NDC number is used to bill for this package of DHS tar gel coal .005 g/g Shampoo?
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.

Prices are the latest CMS NADAC pharmacy acquisition cost per NDC; per-pack figures are per-unit × pack quantity, shown only when the pack is denominated in the same measure NADAC prices.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Thera-Gel 5 mg/mL 00904-5259-44 Major 251 ml $0.009 — Availability likely —
DHS tar gel .005 g/gthis 00096-0736-22 Person 20.8 g — — FDA listed —
Dhs Tar .005 g/g 00096-0737-04 Person 125.04 g — — FDA listed —
DHS Tar 5 mg/mL 00096-0813-08 Person 240 ml — — FDA listed —
Walgreens Original T-Gel Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 00363-1591-01 Walgreen 1 bottle — — FDA listed —
Meijer T Plus Gel Coal Tar Anti-Dandruff 5 mg/mL 41250-0249-01 Meijer 251 ml — — FDA listed —
Medicasp Anti-Dandruff 5 mg/mL 50066-0040-06 Genomma 1 bottle — — FDA listed —
therapeutic tar anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 50804-0887-01 GOODSENSE 473 ml — — FDA listed —
Family Wellness Therapeutic Tplus PLUS Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 55319-0485-01 FAMILY 251 ml — — FDA listed —
True plus Real Therapeutic T plus Plus Original Strength Tar Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 67385-0702-01 Garcoa, 1 bottle — — FDA listed —
amazon basics therapeutic tar anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 72288-0043-01 AMAZON.COM 473 ml — — FDA listed —
QC Anti Dandruff T Plus 5 mg/mL 75376-0286-08 Guangzhou 236 ml — — FDA listed —
TopCare Therapeutic Anti-Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 76162-0190-01 Topco 251 ml — — FDA listed —
meijer therapeutic t plus plus tar gel dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 79481-0083-01 Meijer 473 ml — — FDA listed —
Equate Therapeutic Dandruff Original Strength Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 79903-0087-01 Wal-Mart 1 bottle — — FDA listed —
Equate Therapeutic Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 5 mg/mL 79903-0291-01 Wal-Mart 1 bottle — — FDA listed —
QC Anti Dandruff T Plus 5 mg/mL 83324-0286-08 Chain 236 ml — — FDA listed —
Pete and Pedro Control Anti Itch Dandruff 62.5 mg/mL 84503-0508-00 PETE 236 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

🏛️
1996
On the market since
Jun 1996
📍
2026
Currently FDA-listed
30 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII 62V75NI93W
    A surfactant derived from coconut oil that helps cleanse and remove oils from skin or hair. In medicines and personal care products, it acts as a cleanser and foaming agent.
  • UNII RN3152OP35
    Hypromellose is a plant-based thickener and film-former derived from cellulose. In medicines, it's used to create coatings on tablets and capsules, control how fast the drug dissolves, and improve the product's texture and stability.
  • UNII 7JNC8VN07M
    A synthetic compound made from polyethylene glycol combined with stearic acid. It acts as an emulsifier and surfactant to help mix oil and water-based ingredients and improve how the medicine spreads or dissolves.
  • 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 E8458C1KAA
    A synthetic detergent and cleansing agent derived from lauric acid. It helps break down oils and improve how active ingredients mix into the formula, and may also serve as a foaming or emulsifying agent in topical preparations.
  • 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.

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

The official label also statesPurified Water Triethanolamine Laurel Sulfite Cocamidopropyl Hydroxysultaint Sodium Chloride PEG-8 Distearate Hypromellose 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 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.

Manufacturer & labeler

LabelerPerson and Covey
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code00096
First marketedJun 1996
Product typeHuman Otc Drug
Portfolio23 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.

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 18 words ▾

Indications and use Helps prevent recurrence of scalp itching and flaking associated with Psoriasis, Seborrheic Dermatitis and Dandruff.

⏱️ Dosage and Administration 46 words ▾

Dosage and administration Wet hair thoroughly, apply a liberal amount of shampoo and massage into lather. Allow lather to remain on scalp for several minutes. Rinse hair well and repeat application. For best results use at least twice a week or as directed by a physician.

⚠️ Warnings 137 words ▾

WARNINGS AND PRECAUTIONS SECTION For external use only. Ask a physician before use if you have Psoriasis or Seborrheic Dermatitis that covers a large area of the body. Do not get into eyes.

If contact occurs, rinse eyes thoroughly with water. Use caution in exposing skin to sunlight after applying this product. It may increase your tendency to sunburn for up to 24 hours after application.

Do not use for prolonged periods without consulting a physician. Do not use this product with other forms of Psoriasis therapy such as ultraviolet radiation or prescription drugs, unless directed to do so by a physician. In rare instances, discoloration of gray, blond tinted or bleached hair may occur.

Stop use and ask physician if condition worsens or does not improve after regular use. Store away from excessive heat or cold.

🧪 Active Ingredient 7 words ▾

OTC - ACTIVE INGREDIENT SECTION Coal Tar

🧪 Inactive Ingredients 17 words ▾

INACTIVE INGREDIENT SECTION Purified Water Triethanolamine Laurel Sulfite Cocamidopropyl Hydroxysultaint Sodium Chloride PEG-8 Distearate Hypromellose Citric Acid

🎯 Purpose 9 words ▾

Purpose Controls symptoms of Psoriasis, Seborrheic Dermatitis and Dandruff.

📄 Keep Out of Reach of Children 21 words ▾

Keep out of the reach of children Yes. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 11 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL DHS Tar Gel Sample Tar Gel Shampoo

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

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 DHS tar gel (this brand).

Top reported reactions

Psoriasis420
Malaise300
Fatigue267
Pain252
Nasopharyngitis236
Skin Exfoliation227
Fall223

Age at onset

Child1
Adult62
Elderly66

Reporter sex

758 reports
Male · 36%
Female · 64%

Serious outcomes

Hospitalization351
Life-threatening244
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 113 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.

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 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 Person and Covey. 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 249.6 g (00096-0736-08). 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?
Person and Covey 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.
← 00096-0735-08 · Person 00096-0737-04 · Person →
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.