Sulfur 8 Medicated Dandruff with Salicylic Acid
- Product NDC
- 12022-039
- 11-digit product format
- 120220039
- Labeler code
- 12022
- Product ID
- 12022-039_09735fbf-7789-ca3f-e063-6294a90a9f94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SALICYLIC ACID
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- J. Strickland and Co.
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-01
- 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 Medicated Dandruff with Salicylic Acid
- 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 | 205104 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 12022-039-00 | Sulfur 8 Medicated Dandruff with Salicylic Acid | 222 mL in 1 BOTTLE | LIQUID | 222 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12022-039 | SULFUR 8 MEDICATED DANDRUFF WITH SALICYLIC ACID (SALICYLIC ACID) LIQUID [J. STRICKLAND AND CO.] | 2 | Current NDC, 1 package rows | 20231106_14f41263-9999-448d-a479-abf67fb3b27b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 12022-039-00 | 12022003900 | 222 mL in 1 BOTTLE (12022-039-00) | 222 ml | 2023-10-01 | No | No | Historical |