PCXX NEUTRAL RMS BUBBLEGUM
- Manufacturer
- Ross Healthcare Inc.
- Effective date
- 2025-11-06
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 10
- Source
- full-release
- Hydrated at
- 2026-05-31 22:04:31
Label at a glance#
ProductPCXX NEUTRAL RMS BUBBLEGUM
Active ingredientSODIUM FLUORIDE
Label structure2 sections
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1600786 | PCxx Neutral Rinse 2 % Mouthwash | PSN | 10 |
| 251960 | sodium fluoride 2 % Oral Rinse | PSN | 10 |
| 1600786 | sodium fluoride 20 MG/ML Mouthwash [PCxx Neutral Rinse] | SBD | 10 |
| 251960 | sodium fluoride 20 MG/ML Mouthwash | SCD | 10 |
| 1600786 | PCxx Neutral Rinse 2 % Mouthwash | SY | 10 |
| 1600786 | PCxx Neutral Rinse 20 MG/ML Mouthwash | SY | 10 |
| 251960 | sodium fluoride 2 % Oral Rinse | SY | 10 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62007-213-64 | 2021-01-31 | C162847 | 48780-1 | ba0f9c33-3a6e-a910-e053-dadaa90a0b85 | 37f90a0f-2c67-456b-997e-8a8a4f5f09d3 |
| 62007-213-64 | 2021-01-31 | C162847 | 48780-1 | ba0f9c33-3a6e-a910-e053-dadaa90a0b85 | PCXX NEUTRAL RNS BUBBLEGUM |
| 62007-213-64 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-3a6e-a910-e053-dadaa90a0b85 | 37f90a0f-2c67-456b-997e-8a8a4f5f09d3 |
| 62007-213-64 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-3a6e-a910-e053-dadaa90a0b85 | PCXX NEUTRAL RNS BUBBLEGUM |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62007-213-64 | PCXX NEUTRAL RMS BUBBLEGUM | 1900 mL in 1 BOTTLE, PLASTIC | RINSE | 1900 | 10 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| SODIUM FLUORIDE | ACTIVE INGREDIENT | 8ZYQ1474W7 | 1 | |
| FLUORIDE ION | ACTIVE MOIETY | Q80VPU408O | 1 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | 1 |
Products#
Every source-derived product name is available through these pages.
- PCXX NEUTRAL RMS BUBBLEGUM
- FLUORIDE TREATMENT
- FD&C RED NO. 40
- SODIUM FLUORIDE
- FLUORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 62007-213 | 62007-213-64 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| SODIUM FLUORIDE | 8ZYQ1474W7 | ACTIM |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 9 | 2025-09-18 | full-release | 2026-05-31 21:43:27 |
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| FD&C RED NO. 40 | FD&C RED NO. 40 | WZB9127XOA | SHAMPOO / TOPICAL | 2 mg | ||
| FD&C RED NO. 40 | FD&C RED NO. 40 | WZB9127XOA | SPONGE / TOPICAL | NA | ||
| FD&C RED NO. 40 | FD&C RED NO. 40 | WZB9127XOA | SPONGE / TOPICAL | NA | ||
| FD&C RED NO. 40 | FD&C RED NO. 40 | WZB9127XOA | SOLUTION / DENTAL | NA | ||
| FD&C RED NO. 40 | FD&C RED NO. 40 | WZB9127XOA | SOLUTION / DENTAL | NA | ||
| FD&C RED NO. 40 | FD&C RED NO. 40 | WZB9127XOA | SHAMPOO / TOPICAL | 2 mg |
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 |
|---|---|---|---|---|---|---|
| PCXX NEUTRAL RMS BUBBLEGUM | FLUORIDE TREATMENT | Ross Healthcare Inc. | 37f90a0f-2c67-456b-997e-8a8a4f5f09d3 | 2025-11-06 | Warnings | 62007-213-64 62007-213 62007021364 42f533f7-38db-8940-e063-6394a90ab1b9 37f90a0f-2c67-456b-997e-8a8a4f5f09d3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

