Sulfur 8 Scalp Therapy Medicated Dandruff Control
- Product NDC
- 12022-032
- 11-digit product format
- 120220032
- Labeler code
- 12022
- Product ID
- 12022-032_0834eb14-2e95-ef47-e063-6294a90ad922
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SALICYLIC ACID
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- J. Strickland and Co.
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-01-01
- Substance
- SALICYLIC ACID
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sulfur 8 Scalp Therapy Medicated Dandruff Control
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 1048903 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 12022-032-00 | Sulfur 8 Scalp Therapy Medicated Dandruff Control | 355 mL in 1 BOTTLE | SPRAY | 355 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12022-032 | SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL (SALICYLIC ACID) SPRAY [J. STRICKLAND AND CO.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231021_961ffab9-4e1b-83f3-e053-2a95a90af5fe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 12022-032-00 | 12022003200 | 355 mL in 1 BOTTLE (12022-032-00) | 355 ml | 2020-01-01 | 0000-00-00 | No | No | Current |