warnings
WARNINGS Consult a physician for use in children under 6 years of age. Contact a doctor if symptoms persist.
Digest Ease Difficult Digestion
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Digest Ease Difficult Digestion
- Generic name
- BERBERIS VULGARIS 3C, CARDUUS MARIANUS 3C, CHELIDONIUM MAJUS 3C, NUX VOMICA 5C, ROBINIA PSEUDOACACIA 3C, TARAXACUM OFFICINALE 3C
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54ffc26a-5b77-7b7d-e063-6394a90aabf4
- SPL ID
- 594f5553-dd2e-4799-e063-6394a90acee0
- Version
- 3
- Effective date
- 2026-08-18
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:29
| Harmonized routes |
|---|
| BUCCAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Digest Ease Difficult Digestion | openfda.brand_name | |
| generic name | BERBERIS VULGARIS 3C, CARDUUS MARIANUS 3C, CHELIDONIUM MAJUS 3C, NUX VOMICA 5C, ROBINIA PSEUDOACACIA 3C, TARAXACUM OFFICINALE 3C | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-7007-1 | openfda.package_ndc |
| ndc | package | 76472-7007-2 | openfda.package_ndc |
| ndc | product | 76472-7007 | openfda.product_ndc |
| ndc11 | package | 76472700702 | derived:openfda.package_ndc |
| ndc11 | package | 76472700701 | derived:openfda.package_ndc |
| spl id | 594f5553-dd2e-4799-e063-6394a90acee0 | id | |
| spl set id | 54ffc26a-5b77-7b7d-e063-6394a90aabf4 | set_id | |
| unii | 7E889U5RNN | openfda.unii | |
| unii | 7C42E2D7B0 | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 1TH8Q20J0U | openfda.unii | |
| unii | U946SH95EE | openfda.unii | |
| unii | 7TPC058OWY | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.