Firefly Anticavity Fluoride
- Product NDC
- 66923-003
- 11-digit product format
- 669230003
- Labeler code
- 66923
- Product ID
- 66923-003_bcec5748-5675-4b7b-b844-2ffbac08e719
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- sodium fluoride
- Dosage form
- RINSE
- Route
- DENTAL
- Labeler
- Ranir LLC
- Application
- M008
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-06-16
- Substance
- SODIUM FLUORIDE
- Active strength
- .5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 package | package | 66923-003 | 66923-003-34 | 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 | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Firefly Anticavity Fluoride
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .5 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 8ZYQ1474W7 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 240698 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| e91ed8a1-0d45-402c-9c16-1ae72e695a37 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 66923-003-34 | Firefly Anticavity Fluoride | 237 mL in 1 BOTTLE | RINSE | 237 | 2 | |
| 66923-003-43 | Firefly Anticavity Fluoride | 473 mL in 1 BOTTLE | RINSE | 473 | 2 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Stomach Relief Regular Strength | BISMUTH SUBSALICYLATE | CARDINAL HEALTH 110, LLC. DBA LEADER | 7d6047a9-5557-487a-ae06-f904dac626c9 | 2025-10-14 | Warnings | M008 |
| Stomach Relief Regular Strength | BISMUTH SUBSALICYLATE | Atlantic Biologicals Corp | 401f8393-680c-e1a8-e063-6394a90a81ab | 2025-10-01 | Warnings | M008 |
| First Aid Direct Peptum Tabs | BISMUTH SUBSALICYLATE | Cintas Corp | dd14cd57-3f7c-4634-9da9-6f83dc5bae12 | 2025-09-29 | Warnings | M008 |
| RIGHT REMEDIES Stomach Relief BISMUTH SUBSALICYLATE 262 mg softgel | BISMUTH SUBSALICYLATE | Strive Pharmaceuticals Inc. | 0f271054-fa96-4475-8279-65f4565aba36 | 2025-09-22 | Warnings | M008 |
| Bismuth Subsalicylate Suspension Regular Strength | BISMUTH SUBSALICYLATE | FSA Store Inc. (Caring Mill) | fbabc313-600a-4722-9948-1a3e21414059 | 2025-09-18 | Warnings | M008 |
| QUALITY CHOICE ULTRA STRENGTH STOMACH RELIEF | BISMUTH SUBSALICYLATE | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) | 67c610b1-fe94-4ad3-ad1a-8bd93a4da9d9 | 2025-09-11 | Warnings | M008 |
| Medique Diotame | BISMUTH SUBSALICYLATE | Unifirst First Aid Corporation | 0667ec26-c2cd-153c-e054-00144ff88e88 | 2025-09-08 | Warnings | M008 |
| McKesson Bismuth | BISMUTH SUBSALICYLATE | McKesson Medical-Surgical | d1f3dfa4-e021-6384-e053-2995a90a7b42 | 2025-09-08 | Warnings | M008 |
| Medi-First Pep-T-Med | BISMUTH SUBSALICYLATE | Unifirst First Aid Corporation | 88f4d5d4-92ed-40ab-97a9-181da72f869b | 2025-09-08 | Warnings | M008 |
| Thompson Chewable Bismuth Tabs | BISMUTH SUBSALICYLATE | Thompson Safety LLC | c94b9bc2-b764-a9a7-e053-2a95a90aed81 | 2025-09-08 | Warnings | M008 |
| Goodsense Regular strength Stomach Relief 122 | BISMUTH SUBSALICYLATE | Preferred Pharmaceuticals Inc. | f0588ab8-d1fc-419a-8d68-bee42332d50f | 2025-08-01 | Warnings | M008 |
| Ultra Strength Stomach Relief | BISMUTH SUBSALICYLATE 525 MG | Retail Business Services, LLC. | 338ca589-91ff-30ed-e063-6294a90a243a | 2025-07-21 | Warnings | M008 |
| Regular Strength Stomach Relief | BISMUTH SUBSALICYLATE 525 MG | Retail Business Services, LLC. | 338d61af-35a8-fba7-e063-6294a90a38e8 | 2025-07-21 | Warnings | M008 |
| Senna | SENNOSIDES | Major Pharmaceuticals | cfb6bf89-c77e-4372-9bc9-44d6a659c955 | 2025-07-18 | Warnings | M008 |
| Major Bismuth Subsalicylate | BISMUTH SUBSALICYLATE | Major Pharmaceuticals | 2a7c9cc1-206e-4018-b89d-7b634df43df6 | 2025-07-11 | Warnings | M008 |
| Stomach Relief Regular Strength | BISMUTH SUBSALICYLATE | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 55440401-f82f-45a3-ba7e-6ccdfdacead3 | 2025-07-10 | Warnings | M008 |
| Upset Stomach Relief-Bismuth Subsalicylate 262 mg | BISMUTH SUBSALICYLATE 262 MG | Pioneer Life Sciences, LLC | 07e2cc82-ab0e-46c5-863b-67658b612678 | 2025-06-27 | Warnings | M008 |
| Upset Stomach Relief-Bismuth Subsalicylate 262 mg | BISMUTH SUBSALICYLATE 262 MG | NUVICARE LLC | 6697e464-00ac-41de-a7ea-d7bb24ed5e2a | 2025-06-25 | Warnings | M008 |
| Stomach Relief Regular Strength | BISMUTH SUBSALICYLATE | P & L Development, LLC | 8383945f-b3a7-4242-bfaa-acf24b66406d | 2025-05-30 | Warnings | M008 |
| 5-Symptom Digestive Relief | BISMUTH SUBSALICYLATE | TARGET CORPORATION | 28fba615-48ca-8d96-e063-6394a90a2797 | 2025-04-12 | Warnings | M008 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 240698 | sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse | PSN | e91ed8a1-0d45-402c-9c16-1ae72e695a37 | 2 |
| 240698 | sodium fluoride 0.5 MG/ML Mouthwash | SCD | e91ed8a1-0d45-402c-9c16-1ae72e695a37 | 2 |
| 240698 | sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse | SY | e91ed8a1-0d45-402c-9c16-1ae72e695a37 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 66923-003-34 | 66923000334 | 237 mL in 1 BOTTLE (66923-003-34) | 237 ml | 2021-11-05 | 0000-00-00 | No | No | Current |
| 66923-003-43 | 66923000343 | 473 mL in 1 BOTTLE (66923-003-43) | 473 ml | 2021-06-16 | 0000-00-00 | No | No | Current |