NDC 73656-004 - WHITE GLO MICELLAR
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
- 73656-004
- Package NDCs from labels
- 73656-004-00
- 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 |
|---|---|---|---|
| WHITE GLO MICELLAR - 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 |
|---|---|---|---|---|---|---|
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| Leader Ultra Lubricating Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Cardinal Health | d7f011a2-05ba-47c3-9519-d31602e105c7 | 2026-03-12 | Warnings | 6DC9Q167V3 |
| Leader Restorative Formula Lubricant Eye Drops | PROPYLENE GLYCOL | Cardinal Health | 87fef7e4-e5a8-4aad-94d2-f80f34826d97 | 2026-03-12 | Warnings | 6DC9Q167V3 |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | e874118f-b4fe-4c80-aece-99ea20e7e805 | 2026-03-12 | Warnings | H0G9379FGK |
| Medicated Pain Relief Patch | CAMPHOR, MENTHOL, METHYL SALICYLATE | Kroger Company | 47cc4b05-a937-4624-bf41-85b8bd7c049e | 2026-03-12 | Warnings | LAV5U5022Y |
| Alka-Seltzer Heartburn Plus Gas ReliefChews Tropical Punch | CALCIUM CARBONATE AND SIMETHICONE | Bayer HealthCare LLC. | 41d17406-3653-4889-81df-6270b7b5d3c7 | 2026-03-12 | Warnings | H0G9379FGK |
| AMAZON Ultra Strength Tropical Fruit | ANTACID TABLETS (CALCIUM CARBONATE) | AMAZON.COM SERVICES LLC | dd93a70e-8b43-495e-bda3-526e5d6de953 | 2026-03-12 | Warnings | H0G9379FGK |
| complete dual action | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | HyVee Inc | 237efe92-b302-4e11-93fe-7b0f727a00aa | 2026-03-12 | Warnings | H0G9379FGK |
| Stance | 0.63% STANNOUS FLUORIDE CONCENTRATE RINSE | Elevate Oral Care | 3ae8badf-f960-62fd-e054-00144ff8d46c | 2026-03-11 | Warnings | M021 |
| Stance | 0.63% STANNOUS FLUORIDE CONCENTRATE RINSE | Elevate Oral Care | 3ae71258-a8c2-6eb5-e054-00144ff88e88 | 2026-03-11 | Warnings | M021 |
| Optimel Manuka Dry Eye Drops | GLYCERIN | Melcare Biomedical Pty Ltd | 88c5e2f0-9f7e-62d1-e053-2995a90a9014 | 2026-03-11 | Warnings | PDC6A3C0OX |
| Optimel Manuka Forte Eye Gel | GLYCERIN | Melcare Biomedical Pty Ltd | 8e0ed6e8-51fc-7c5b-e053-2a95a90a35a9 | 2026-03-11 | Warnings | PDC6A3C0OX |
| Delta Travel Kit Comfort plus | SODIUM MONOFLUOROPHOSPHATE | Buzz Products Inc. | d31e0920-4317-1e0c-e053-2a95a90aebeb | 2026-03-11 | Warnings | M021 545626 |
| Anticavity Fluoride Rinse | SODIUM FLUORIDE | CVS Pharmacy, Inc. | eac346d9-d9c1-4417-8193-390c7a0dcc2a | 2026-03-10 | Warnings, Adverse reactions | M021 |
| Crest Cavity Protection Regular | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 6caf3f2e-70a2-4530-99fa-f5af7e4c511a | 2026-03-10 | Warnings | M021 |
| Amerfresh Toothpowder | SODIUM FLUORIDE | Yangzhou ONE & ONLY Personal Care Products Co., LTD | 1cacf93e-aa60-4717-87ab-0568a701a4f3 | 2026-03-10 | Warnings | M021 |
| Anticavity | SODIUM FLUORIDE | CVS Pharmacy, Inc. | a51357df-6d55-4030-a5db-42da7ba54a37 | 2026-03-09 | Warnings, Adverse reactions | M021 |
| Fleet | GLYCERIN | C.B. Fleet Company, Inc. | 31778652-e60e-4098-8e90-3e4f56b5800c | 2026-03-06 | Warnings | PDC6A3C0OX |
| Glycerin | GLYCERIN | Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd | 4c6094b7-c1ef-26a3-e063-6394a90af4cc | 2026-03-06 | Warnings | PDC6A3C0OX |
| Rain Renewal Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Rain Eye Drops, LLC | bb451b22-c4f6-291d-e053-2a95a90a7801 | 2026-03-06 | Warnings | K679OBS311 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.