RITE AID RENEWAL
- Product NDC
- 11822-6181
- 11-digit product format
- 118226181
- Labeler code
- 11822
- Product ID
- 11822-6181_5a0c253c-a39f-46e0-a7be-65bec449a4a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SELENIUM SULFIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RITE AID CORPORATION
- Application
- part358H
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-03-26
- Marketing end
- 0000-00-00
- Substance
- SELENIUM SULFIDE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11822-6181-3 | Daylogic Maximum Strength Dandruff | 420 mL in 1 BOTTLE, PLASTIC | LIQUID | 420 | | 1 |
| 11822-6181-4 | RITE AID RENEWALCLINICAL | 420 mL in 1 BOTTLE, PLASTIC | LIQUID | 420 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-6181 | DAYLOGIC MAXIMUM STRENGTH DANDRUFF (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION] | 1 | Legacy NDC, 1 package rows | 20160211_b5e3550a-de63-42b5-90d3-5c23cca941c6.zip |
| 11822-6181 | RITE AID RENEWAL CLINICAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION] | 1 | Legacy NDC, 1 package rows | 20130529_46544d34-8126-4b42-beff-d202523d4d54.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11822-6181-3 | 11822618103 | 420 mL in 1 BOTTLE, PLASTIC | 420 ml | Historical |
| 11822-6181-4 | 11822618104 | 420 mL in 1 BOTTLE, PLASTIC | 420 ml | Historical |