Sulfur 8 Fresh Anti-Dandruff
- Product NDC
- 12022-028
- 11-digit product format
- 120220028
- Labeler code
- 12022
- Product ID
- 12022-028_0833ce8a-3b6d-7ca8-e063-6394a90afc4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- J. Strickland & Co.
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2008-02-06
- 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 Fresh Anti-Dandruff
- 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 | 251577 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 12022-028-00 | Sulfur 8 Fresh Anti-Dandruff | 355 mL in 1 BOTTLE | SOLUTION | 355 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12022-028 | SULFUR 8 FRESH ANTI-DANDRUFF (SALICYLIC ACID) SOLUTION [J. STRICKLAND & CO.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231101_5acd1aab-3a6d-4d2c-8c80-271ab8dcac1a.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 |
|---|
| 12022-028-00 | 12022002800 | 355 mL in 1 BOTTLE (12022-028-00) | 355 ml | 2008-02-06 | 0000-00-00 | No | No | Current |