Salicylic Acid
- Product NDC
- 11822-0120
- Requested package NDC
- 11822-0120-9
- 11-digit product format
- 118220120
- Labeler code
- 11822
- Product ID
- 11822-0120_c7928aa7-b345-b3bf-e053-2995a90a5167
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Corn and Callus Remover Liquid
- 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 mg/9.8mL
- 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 |
|---|
| 11822-0120-9 | Salicylic Acid | 9.8 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 9.8 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0120 | SALICYLIC ACID (CORN AND CALLUS REMOVER LIQUID) LIQUID [RITE AID CORPORATION] | 9 | Legacy NDC, 1 package rows | 20241213_ea071f97-c4ba-4283-b372-9f4292ad9b2c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0120-9 | 11822012009 | 9.8 mL in 1 BOTTLE, WITH APPLICATOR (11822-0120-9) | 9.8 ml | 2017-12-22 | 0000-00-00 | No | No | Current |