NDC 47682-008-99 - Green Guard Stomach Relief
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
- 47682-008
- Requested NDC
- 47682-008-99
- Package NDCs from labels
- 47682-008-99, 47682-008-33, 47682-008-48
- Manufacturer
- Unifirst First Aid Corporation | Prestige Packaging
- Effective date
- 2020-07-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Green Guard Stomach Relief - Unifirst First Aid Corporation | Prestige Packaging | Unifirst First Aid Corporation | Prestige Packaging | 2020-07-21 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Calcium Carbonate | ACTIVE INGREDIENT | H0G9379FGK | GREEN GUARD STOMACH RELIEF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNIFIRST FIRST AID CORPORATION] | 3 | |
| Carbonate Ion | ACTIVE MOIETY | 7UJQ5OPE7D | GREEN GUARD STOMACH RELIEF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNIFIRST FIRST AID CORPORATION] | 3 | |
| ACACIA | INACTIVE INGREDIENT | 5C5403N26O | GREEN GUARD STOMACH RELIEF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNIFIRST FIRST AID CORPORATION] | 3 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | GREEN GUARD STOMACH RELIEF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNIFIRST FIRST AID CORPORATION] | 3 | |
| MALTODEXTRIN | INACTIVE INGREDIENT | 7CVR7L4A2D | GREEN GUARD STOMACH RELIEF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNIFIRST FIRST AID CORPORATION] | 3 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | GREEN GUARD STOMACH RELIEF (CALCIUM CARBONATE) TABLET, CHEWABLE [UNIFIRST FIRST AID CORPORATION] | 3 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.