Compound W
- Product NDC
- 51142-595
- 11-digit product format
- 511420595
- Labeler code
- 51142
- Product ID
- 51142-595_0a342930-143d-3e10-e063-6394a90aeb8e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic acid gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ASO LLC
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-12-01
- Marketing end
- 2029-02-20
- Substance
- SALICYLIC ACID
- Active strength
- 170 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Compound W
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 170 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 210140, 312880 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51142-595-12 | Compound W | 7 g in 1 TUBE | GEL | 7 | | 5 |
| 51142-595-12 | Compound W | 1 in 1 CARTON | GEL | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51142-595 | COMPOUND W (SALICYLIC ACID GEL) GEL [ASO LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20231116_b55c7421-a8fe-8d4e-e053-2a95a90a7a6f.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 |
|---|
| 51142-595-12 | 51142059512 | 1 TUBE in 1 CARTON (51142-595-12) / 7 g in 1 TUBE | 1 tube | 2020-12-01 | 0000-00-00 | No | No | Current |