Dandruff Relief
- Product NDC
- 11822-1237
- 11-digit product format
- 118221237
- Labeler code
- 11822
- Product ID
- 11822-1237_146a62ff-ed84-44f7-a94e-f44003b08d06
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid 3.0%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Rite Aid
- Application
- part358H
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-09-30
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11822-1237-3 | Dandruff Reliefdaylogic | 74 mL in 1 BOTTLE | LIQUID | 74 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-1237 | DANDRUFF RELIEF DAYLOGIC (SALICYLIC ACID 3.0%) LIQUID [RITE AID] | 1 | Legacy NDC, 1 package rows | 20180622_8d173e79-6459-4545-84fe-d9817a309b69.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11822-1237-3 | 11822123703 | 74 mL in 1 BOTTLE | 74 ml | Historical |