Glister Multi-Action Fluoride
- Product NDC
- 10056-530
- 11-digit product format
- 100560530
- Labeler code
- 10056
- Product ID
- 10056-530_b51834c4-f409-6079-e053-2a95a90acc94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- TOPICAL
- Labeler
- Access Business Group, LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-04-11
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 10056-530 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 10056-530 | 10056-530-06 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 10056-530 | 10056-530-65 | D | Discontinued by firm | 2026-10-05 |
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.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | 10056-530 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | ||
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 10056-530 | 10056-530-06 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 10056-530 | 10056-530-65 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 10056-530-06 | 10056053006 | 1 TUBE in 1 BOX (10056-530-06) > 191 g in 1 TUBE | 1 tube | 2011-04-11 | 0000-00-00 | No | No | Current |
| 10056-530-65 | 10056053065 | 1 TUBE in 1 BOX (10056-530-65) > 65 g in 1 TUBE | 1 tube | 2011-04-11 | 0000-00-00 | No | No | Current |