Ludens Wild Honey Throat Drops
- Product NDC
- 52183-239
- 11-digit product format
- 521830239
- Labeler code
- 52183
- Product ID
- 52183-239_4a0e60eb-f121-41b2-8a50-0a4638850efc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pectin
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Prestige Brands Holdings, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-07-08
- Marketing end
- 0000-00-00
- Substance
- PECTIN
- Active strength
- 3 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 52183-239 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 52183-239 | 52183-239-30 | D | Discontinued by firm | | 2026-07-31 |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
Warnings When using this product do not use longer than four weeks unless recommended by a dentist
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52183-239-30 | 52183023930 | 30 LOZENGE in 1 BAG (52183-239-30) | 30 lozenge | 2010-07-08 | 0000-00-00 | No | No | Current |