NDC 73656-012 - WHITE GLO CHARCOAL SENSITIVE
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 73656-012
- Package NDCs from labels
- 73656-012-00
- Manufacturer
- WHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,Ltd
- Effective date
- 2025-02-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SORBITOL - WHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,Ltd | WHITE GLO USA INC | Suzhou Baozi Healthy Technology Co.,Ltd | 2025-02-26 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73656-012-00 | WHITE GLO CHARCOAL SENSITIVE | 1 in 1 TUBE | PASTE, DENTIFRICE | 50 mg in 1g | 6 | |
| 73656-012-00 | WHITE GLO CHARCOAL SENSITIVE | 150 g in 1 BOX | PASTE, DENTIFRICE | 150 g | 50 mg in 1g | 6 |
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 |
|---|---|---|---|---|---|---|
| Ionite H | SODIUM FLUORIDE, POTASSIUM NITRATE | Dharma Research, Inc. | 642fec99-c5c5-4ef2-986e-5b5f7cf460de | 2015-08-02 | Warnings, Adverse reactions | RU45X2JN0Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.