NDC 73656-016 - White Glo Instant White
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
- 73656-016
- Package NDCs from labels
- 73656-016-00
- 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 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 |
|---|---|---|---|---|---|---|
| Crest Complete Multi-Benefit Whitening plus Scope | SODIUM FLUORIDE | Procter & Gamble Manufactura, S. de R.L. de C.V. | 0206710a-707f-4aa9-96b9-86240c1275dc | 2026-04-28 | Warnings | M021 |
| Alcohol Free Refreshing Mint | SODIUM FLUORIDE | H E B | cedf7c08-7412-4733-9b67-225b331cec8c | 2026-04-27 | Warnings, Adverse reactions | M021 |
| anzoon ANTIBACTERIAL MOUTH WASH | CETYLPYRIDINIUM CHLORIDE | Shandong AZC Biotechnology Co.,Ltd. | 507c6896-2806-790c-e063-6394a90ac5ce | 2026-04-27 | Warnings | M021 |
| REFRESH TEARS PF | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Allergan, Inc. | 9e1cba7b-84ed-47f3-b19a-121992834350 | 2026-04-24 | Warnings | K679OBS311 |
| DELTA COMFORT PLUS AMENITY | SODIUM MONOFLUOROPHOSPHATE | Buzz Products Inc. | 26434794-ae02-0f58-e063-6294a90ad85e | 2026-04-24 | Warnings | M021 545626 |
| A and H Plus Therabreath Breath Freshners | SODIUM FLUORIDE | Church & Dwight Co., Inc. | 18d6073e-b1ee-47d2-9758-2cf04f3cf3ca | 2026-04-23 | Warnings | M021 |
| Fluoride | SODIUM FLUORIDE | McKesson | 5025e58e-e59c-07b6-e063-6394a90ac1e8 | 2026-04-23 | Warnings | M021 |
| PRO-SYS | SENSITIVITY - MINT (OTC) | Benco Dental | 4e46847e-8c1d-c988-e063-6394a90a8e50 | 2026-04-22 | Warnings | M021 |
| Anticavity Fluoride Rinse | SODIUM FLUORIDE | H E B | 87327a36-a314-4daa-83b6-b4bd3e26bba2 | 2026-04-22 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | H E B | 8df324a7-9204-40f3-8ddb-1656286d7d4e | 2026-04-22 | Warnings, Adverse reactions | M021 |
| Colgate Total SF Whitening | STANNOUS FLUORIDE | Colgate-Palmolive Company | 3bba340e-2a62-3b04-41b5-0ed9c13adb13 | 2026-04-22 | Warnings | M021 |
| EverSmile Squirt | SODIUM FLUORIDE 0.05% | Everbrands, Inc. | bc0ef174-2909-469a-b629-0eab4412bdfc | 2026-04-20 | Warnings | M021 |
| Gum Detoxify | STANNOUS FLUORIDE | Walmart | 41d6cc7a-0b87-e474-e063-6294a90ae995 | 2026-04-20 | Warnings | M021 |
| Eversmile Squirt | 2.65% HYDROGEN PEROXIDE | Everbrands, Inc. | 2c43dedf-eeb0-43ba-a352-3d56ffd9d6cf | 2026-04-19 | Warnings | M021 |
| Alcohol-Free Anticavity | SODIUM FLUORIDE | H E B | 8d40f693-083c-4eb6-9da1-42675d757e0e | 2026-04-16 | Warnings, Adverse reactions | M021 |
| Eversmile OrthoFoam Anticavity | 0.05% SODIUM FLUORIDE RINSE | Everbrands, Inc. | 9c12e792-94c8-4e29-9a54-e7e70aadade6 | 2026-04-16 | Warnings | M021 |
| Eversmile Squirt | 2.65% HYDROGEN PEROXIDE | Everbrands, Inc. | 6753b426-6d49-4438-a52f-c28e60a0e9d8 | 2026-04-16 | Warnings | M021 |
| Osstem G Gum Health Care Tooth | SODIUM FLUORIDE | Osstem Pharma Co., Ltd | 4f8b4fc0-4c98-5e52-e063-6394a90af710 | 2026-04-15 | Warnings | M021 |
| Crest 3D White Deep Stain Remover Enamel Strength | SODIUM MONOFLUOROPHOSPHATE | The Procter & Gamble Manufacturing Company | 4f6b8851-c778-8abd-e063-6294a90aef4f | 2026-04-14 | M021 C810JCZ56Q | |
| Crest 3D White Stain Eraser Luxe Mint | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 4f6beb3b-2521-bfb7-e063-6394a90ad9ea | 2026-04-14 | M021 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.