warnings
WARNINGS: IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor. KEEP OUT OF REACH OF CHILDREN.
Lyme Disease Support 2
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
- Lyme Disease Support 2
- Generic name
- ARGENTUM NITRICUM, ASTRAGALUS MENZIESII, CALCAREA SULPHURICA, CUPRUM ARSENICOSUM, DNA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI SULPHURICUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RNA, SILICEA.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 13b4b78b-f9f7-4cf6-8f43-61679160086b
- SPL ID
- d44b323b-0822-b3d4-e053-2995a90aafb7
- Version
- 4
- Effective date
- 2021-12-29
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:55
| 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 | Lyme Disease Support 2 | openfda.brand_name | |
| generic name | ARGENTUM NITRICUM, ASTRAGALUS MENZIESII, CALCAREA SULPHURICA, CUPRUM ARSENICOSUM, DNA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI SULPHURICUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RNA, SILICEA. | openfda.generic_name | |
| manufacturer name | OHM PHARMA INC. | openfda.manufacturer_name | |
| ndc | package | 66096-723-05 | openfda.package_ndc |
| ndc | product | 66096-723 | openfda.product_ndc |
| ndc11 | package | 66096072305 | derived:openfda.package_ndc |
| spl id | d44b323b-0822-b3d4-e053-2995a90aafb7 | id | |
| spl set id | 13b4b78b-f9f7-4cf6-8f43-61679160086b | set_id | |
| unii | 877L01IZ0P | openfda.unii | |
| unii | E934B3V59H | openfda.unii | |
| unii | SK8L60BCSQ | openfda.unii | |
| unii | 51FI676N6F | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 95IT3W8JZE | openfda.unii | |
| unii | 91GQH8I5F7 | openfda.unii | |
| unii | 1K573LC5TV | openfda.unii | |
| unii | NC1P15G4KZ | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | J17GBZ5VGX | 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.