Sebex Antidandruff, anti-seborrheic dermatitis, anti-psoriasis Salicylic Acid, Sulfur 20 mg/1000mL; 20 mg/1000mL Shampoo, 118 mL — NDC 0536-1962-97 (Billing 00536-1962-97)
This is a package of 118 mL of Sebex Antidandruff, anti-seborrheic dermatitis, anti-psoriasis Salicylic Acid, Sulfur 20 mg/1000mL; 20 mg/1000mL Shampoo from Rugby Laboratories, marketed since Oct 2012 and currently FDA-listed; retail pharmacies pay about $0.0225 per mL (NADAC). It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 0536-1962-97 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 0536 labeler · 1962 product · 97 package
- Package marketed since
- Oct 29, 2012
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Billing quantity
- 118 mL per package
- Barcode (UPC-A, from the NDC)
- 3 0536196297 5
- Medicaid fills, this package
- 191 prescriptions in the last four reported quarters
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
- GSN (GCN sequence number): 005754
- GCN: 79591
- GPI-14 (Medi-Span): 90309902104520
- HICL (First Databank): 002461
- AHFS class code: 84:28.00.00
- RxCUI (RxNorm): 204638
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Preparations containing sulfur class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Sebex Antidandruff is an over-the-counter medicated shampoo containing salicylic acid and sulfur. This product is formulated as an OTC monograph drug, meaning it follows FDA's established rules for this category rather than individual approval. Salicylic acid and sulfur are commonly used together in topical products to help reduce scaling, flaking, and irritation associated with conditions like dandruff, seborrheic dermatitis, and psoriasis. The shampoo is applied directly to the scalp and hair during washing.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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 | $0.023 | $2.66 / 118 ml |
| Medicaid paysCMS SDUD · 12 mo | $0.0510 | $6.02 / 118 ml |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file · file of Sep 30, 2026
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · through Q1 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 00536-1962-97 You're viewing this Main listing | 118 mL in 1 BOTTLE | 2012-10-29 | — | Active |
Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Sebex Antidandruff, anti-seborrheic dermatitis, anti-psoriasis 20 mg/1000mL; 20 mg/1000mLthis 00536-1962-97 | Rugby | 118 ml | $0.022 | — | Availability likely | — |
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file · file of Sep 30, 2026
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
What it looks like
Where does this data come from?
- FDA label on DailyMed · label index refreshed Oct 5, 2026
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 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 6K8PRP397M
A plant-derived cleansing agent made from coconut oil. It helps the medicine dissolve evenly and improves how the product spreads or mixes in formulations.
-
UNII F05Q2T2JA0
Docusate sodium is a stool softener compound that helps medicines dissolve and move through the digestive tract. It acts as a surfactant, reducing surface tension in the intestines, and also serves as a wetting agent in tablet formulations.
-
UNII 8CRQ2TH63M
Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
-
UNII 09179OX7TB
PEG-75 Lanolin is a waxy substance derived from sheep's wool that has been chemically modified to mix easily with water and oil. It acts as an emulsifier and moisturizer in topical formulations, helping blend different ingredients and soften the skin.
-
UNII E40U03LEM0
A synthetic preservative that kills bacteria and fungi to keep the medicine from spoiling during storage and use.
-
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 368GB5141J
A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
-
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.
9 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 5, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Rugby Laboratories labeler code 00536
- Olopatadine HCl olopatadine hydrochloride 7 mg/mL Solution/ Drops NDC 0536-1478-23
- Cough Suppressant Adult Dextromethorphan Hydrobromide 15 mg Capsule, Liquid Filled NDC 0536-1480-34
- Athletes Foot Tolnaftate 10 mg/g Aerosol, Spray NDC 0536-1481-01
- Senna 8.8 mg/5mL Solution NDC 0536-1483-59
- Rugby Mucus Relief ER guaifenesin 600 mg Tablet, Multilayer, Extended Release NDC 0536-1489-20
- Rugby Allergy Relief D fexofenadine hydrochloride, pseudoephedrine hydrochloride 60 mg; 120 mg Tablet, Film Coated, Extended Release NDC 0536-1491-07
- Rugby Anti-Dandruff Selenium Sulfide 10 mg/mL Shampoo NDC 0536-1995-53
- MILK OF MAGNESIA MINT magnesium hydroxide 1200 mg/15mL Liquid NDC 0536-2470-85
- Capsaicin .25 mg/g Cream NDC 0536-2525-25
- Rugby Nicotine Polacrilex Gum, Original Flavor 2 mg Gum, Chewing NDC 0536-3029-06
- Rugby Nicotine Polacrilex Gum, Original Flavor 4 mg Gum, Chewing NDC 0536-3030-06
- Rugby Nicotine Polacrilex Gum, Coated Mint Flavor 2 mg Gum, Chewing NDC 0536-3112-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses controls the symptoms of: dandruff seborrheic dermatitis psoriasis
⏱️ Dosage and Administration ▾
Directions SHAKE WELL BEFORE USE wet the scalp or skin and massage in enough shampoo to work up a lather massage for 3-5 minutes and rinse out thoroughly repeat application and rinse thoroughly again for best results, use at least twice a week or as directed by a doctor
⚠️ Warnings ▾
Warnings For external use only Do not use If condition covers a large area of the body, consult your doctor before using this product this product with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs unless directed to do so by a doctor When using this product avoid contact with eyes If contact occurs, rinse eyes thoroughly with water Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
📦 Storage and Handling ▾
Other information store at room temperature see container for Lot No. & Exp. date
🧪 Active Ingredient ▾
Active ingredients Purpose Salicylic Acid, 2% } Sulfur, 2% Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis
🧪 Inactive Ingredients ▾
Inactive ingredients water, sodium lauryl sulfate, disodium cocoamphodipropionate, acrylates copolymer, citric acid, PEG-75 lanolin, fragrance, quaternium-15, diethylhexyl sodium sulfosuccinate, isopropyl palmitate, sodium hydroxide.
🎯 Purpose ▾
Active ingredients Purpose Salicylic Acid, 2% } Sulfur, 2% Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis
📄 Do Not Use ▾
Do not use If condition covers a large area of the body, consult your doctor before using this product this product with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs unless directed to do so by a doctor
📄 When Using This Product ▾
When using this product avoid contact with eyes If contact occurs, rinse eyes thoroughly with water
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.
📄 Keep Out of Reach of Children ▾
KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
📄 Questions or Comments ▾
Questions or comments? 1-800-645-2158
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label Rugby ® NDC 0536-1962-97 Sebex Medicated Dandruff, Seborrheic Dermatitis, and Psoriasis Shampoo 4 FL OZ (118 mL) Principal Display Panel - 118 mL Bottle Label