Salicylic Acid
- Product NDC
- 11822-0119
- Requested package NDC
- 11822-0119-9
- 11-digit product format
- 118220119
- Labeler code
- 11822
- Product ID
- 11822-0119_c792bfb2-83cc-5ec5-e053-2995a90a35df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Liquid Wart Remover
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RITE AID CORPORATION
- Application
- part358F
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-12-22
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 0 g/9mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11822-0119-9 | Salicylic Acid | 9 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0119 | SALICYLIC ACID (LIQUID WART REMOVER) LIQUID [RITE AID CORPORATION] | 8 | Legacy NDC, 1 package rows | 20241213_6f25036a-e55d-4be9-b090-f314b9b45760.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0119-9 | 11822011909 | 9 mL in 1 BOTTLE, WITH APPLICATOR (11822-0119-9) | 9 ml | 2017-12-22 | 0000-00-00 | No | No | Current |