NDC 11822-2000-01 - Simplify White Tea LHS
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 11822-2000
- Requested NDC
- 11822-2000-01
- Package NDCs from labels
- 11822-2000-1, 11822-2000-01
- Manufacturer
- RITE AID CORPORATION | Apollo Health and Beauty Care
- Effective date
- 2026-05-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Simplify White Tea LHS - RITE AID CORPORATION | Apollo Health and Beauty Care | RITE AID CORPORATION | Apollo Health and Beauty Care | 2026-05-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11822-2000-1 | Simplify White Tea LHS | 332 mL in 1 BOTTLE, PLASTIC | LIQUID | 332 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11822-2000 | SIMPLIFY WHITE TEA LHS (BENZALKONIUM CHLORIDE) LIQUID [RITE AID CORPORATION] | 2 | Current NDC, 1 package rows | 20250120_20d72396-2aeb-f8f3-e063-6394a90a9ec8.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.