warnings
Warnings: If pregnant or breast feeding, ask a doctor before using product. Stop use and ask a doctor if symptom persist more than 3 days, worsen, or if new symptom occur. KEEP OUT OF REACH OF CHILDREN.
Immune Booster
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
- Immune Booster
- Generic name
- APIS MELLIFICA, BAPTISIA TINCTORIA, CARDUUS MARIANUS, ECHINACEA ANGUSTIFOLIA, GALLUM APARINE, MERCURIUS CORROSIVUS, MERCURIUS SULPHURATUS RUBER, NITRICUM ACIDUM, SULPHUR IODATUM, THUJA OCCIDENTALIS.
- Manufacturer
- Sunway Biotech LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 9ae14a66-9f6b-4ca8-b335-f6f75ddb8d93
- SPL ID
- d44c13ea-157e-a23c-e053-2995a90a4f07
- Version
- 4
- Effective date
- 2021-12-29
- 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 05:15:19
| Harmonized routes |
|---|
| ORAL |
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 | Immune Booster | openfda.brand_name | |
| generic name | APIS MELLIFICA, BAPTISIA TINCTORIA, CARDUUS MARIANUS, ECHINACEA ANGUSTIFOLIA, GALLUM APARINE, MERCURIUS CORROSIVUS, MERCURIUS SULPHURATUS RUBER, NITRICUM ACIDUM, SULPHUR IODATUM, THUJA OCCIDENTALIS. | openfda.generic_name | |
| manufacturer name | Sunway Biotech LLC | openfda.manufacturer_name | |
| ndc | package | 27281-049-65 | openfda.package_ndc |
| ndc | product | 27281-049 | openfda.product_ndc |
| ndc11 | package | 27281004965 | derived:openfda.package_ndc |
| spl id | d44c13ea-157e-a23c-e053-2995a90a4f07 | id | |
| spl set id | 9ae14a66-9f6b-4ca8-b335-f6f75ddb8d93 | set_id | |
| unii | 411VRN1TV4 | openfda.unii | |
| unii | 1NT28V9397 | openfda.unii | |
| unii | U946SH95EE | openfda.unii | |
| unii | 53GH7MZT1R | openfda.unii | |
| unii | VB06AV5US8 | openfda.unii | |
| unii | 5EF0HWI5WU | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | ZI0T668SF1 | openfda.unii | |
| unii | Z4B6561488 | openfda.unii | |
| unii | L6L8KA2AA0 | 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.