Lucky
- Product NDC
- 20276-045
- 11-digit product format
- 202760045
- Labeler code
- 20276
- Product ID
- 20276-045_ece38500-eec9-3009-e053-2995a90aa441
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pyrithione zinc
- Dosage form
- SHAMPOO
- Route
- TOPICAL
- Labeler
- Delta Brands Inc
- Application
- M032
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-06-30
- Marketing end
- 0000-00-00
- Substance
- PYRITHIONE ZINC
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Dataset | Scope | Package NDC |
|---|---|---|
| excluded product | product | |
| excluded package | package | 20276-045-13 |
| excluded package | package | 20276-045-12 |
| excluded package | package | 20276-045-14 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 20276-045-12 | 2020-12-14 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-13 | 2020-12-14 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-14 | 2020-12-14 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-12 | 2020-09-27 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-13 | 2020-09-27 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-14 | 2020-09-27 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-12 | 2020-09-25 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-13 | 2020-09-25 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-14 | 2020-09-25 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-12 | 2020-07-22 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-13 | 2020-07-22 | DRY HAIR- pyrithione zinc shampoo |
| 20276-045-14 | 2020-07-22 | DRY HAIR- pyrithione zinc shampoo |
DailyMed Socrata Ingredients#
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 20276-045-12 | 20276004512 | 355 mL in 1 BOTTLE, PLASTIC (20276-045-12) | 355 ml | 2012-06-30 | 0000-00-00 | No | No | Current |
| 20276-045-13 | 20276004513 | 400 mL in 1 BOTTLE, PLASTIC (20276-045-13) | 400 ml | 2019-02-01 | 0000-00-00 | No | No | Current |
| 20276-045-14 | 20276004514 | 420 mL in 1 BOTTLE, PLASTIC (20276-045-14) | 420 ml | 2012-06-30 | 0000-00-00 | No | No | Current |