NDC 68703-343 - PetAlive PetCalm
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
- 68703-343
- Package NDCs from labels
- 68703-343-20
- Manufacturer
- SILVER STAR BRANDS
- Effective date
- 2025-12-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PetAlive PetCalm - SILVER STAR BRANDS | SILVER STAR BRANDS | 2025-12-16 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68703-343-20 | PetAlive PetCalm | 29000 mg in 1 BOTTLE, GLASS | GRANULE | 29000 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ReHydration | ADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI PHOSPHORICUM, NATRUM MURIATICUM, SARSAPARILLA, SILICEA, TARAXACUM OFFICINALE, THYROIDINUM (BOVINE) | Energetix Corp | 9883c502-9782-451e-9eec-c54d7b054f31 | 2017-01-31 | Warnings | CI71S98N1Z |
| Enuresis HP | ARGENTUM NITRICUM, BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE, KREOSOTUM, NITRICUM ACIDUM, PULSATILLA (VULGARIS), THUJA OCCIDENTALIS | BioActive Nutritional, Inc. | a6fff9be-e78d-4539-b741-6a8080a164a0 | 2016-09-07 | Warnings | 95IT3W8JZE |
| Cerebroforce | CAPSICUM ANNUUM, GINKGO BILOBA, GELSEMIUM SEMPERVIRENS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, ARSENICUM ALBUM | BioActive Nutritional, Inc | f998ed3f-56a5-4497-be5b-9a819fe8be69 | 2016-07-13 | Warnings | CI71S98N1Z |
| Silver Nitrate | SILVER NITRATE | Teva Pharmaceuticals USA, Inc. | 6956c883-fc1b-49be-97bc-e642e0aa907d | 2016-02-01 | 95IT3W8JZE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.