Dosage and administration
Apply to the affected area one to four times daily or as directed by a doctor. Use after shampooing or between shampoos.
Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment
- Manufacturer
- J. Strickland and Co.
- Effective date
- 2023-10-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:57:07
Label at a glance#
ProductSulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment
Active ingredientSALICYLIC ACID
Label structure6 sections
Label contents#
Full prescribing information#
Active Ingredient
Salicylic Acid, 2%
Purpose
Antidandruff, Seborrheic Dermatitis, Psoriasis
Use:
for relief of scalp itching, irritation, redness, scaling and flaking associated with dandruff, seborrheic dermatitis, psoriasis.
Warnings
For external use only
Ask a doctor before use
if the condition covers a large area of the body.
When using this product
avoid contact with eyes. If contact, rinse eyes thoroughly with water.
Stop use and consult 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 right away.
Keep away from heat and open flame. Flammable
Directions
Apply to the affected area one to four times daily or as directed by a doctor. Use after shampooing or between shampoos.
Inactive Ingredients
Water, SD Alcohol 40, Propylene Glycol, Benzyl Alcohol, Menthol, Fragrance
Package Labeling:
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 12022-033-00 | Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment | 74 mL in 1 BOTTLE | SOLUTION | 74 | 3 | |
| 12022-033-00 | Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment | 1 in 1 BOX | SOLUTION | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 12022-033 | SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL LEAVE-IN SOOTHING TREATMENT (SALICYLIC ACID) SOLUTION [J. STRICKLAND AND CO.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20231021_96b24a6f-3d6e-6d60-e053-2a95a90a8330.zip |
Products#
Every source-derived product name is available through these pages.
- Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment
- SALICYLIC ACID
- WATER
- PROPYLENE GLYCOL
- BENZYL ALCOHOL
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 12022-033 | 12022-033-00 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
| MENTHOL | L7T10EIP3A | IACT |
| SALICYLIC ACID | O414PZ4LPZ | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment | SALICYLIC ACID | J. Strickland and Co. | 96b24a6f-3d6e-6d60-e053-2a95a90a8330 | 2023-10-21 | Warnings | 12022-033-00 12022-033 12022003300 0834f4b7-cad7-182f-e063-6294a90a7faa 96b24a6f-3d6e-6d60-e053-2a95a90a8330 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.