warnings
W arnings: Use only as directed. Stop use and consult a doctor if symptoms worsen or do not improve after 5 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
Mold Relief Formula
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
- Mold Relief Formula
- Generic name
- KALI MURIATICUM, GELSEMIUM, KALI BICHROMICUM, SABADILLA, HISTAMINUM, MOLD MIX.
- Manufacturer
- Integrative Healing Institute, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 067ee707-7219-4370-9cdd-08888f45b5e5
- SPL ID
- 416205c4-4fec-1e12-e063-6294a90af417
- Version
- 6
- Effective date
- 2025-10-17
- Source export date
- 2026-10-30
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:29:33
| 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 | Mold Relief Formula | openfda.brand_name | |
| generic name | KALI MURIATICUM, GELSEMIUM, KALI BICHROMICUM, SABADILLA, HISTAMINUM, MOLD MIX. | openfda.generic_name | |
| manufacturer name | Integrative Healing Institute, LLC | openfda.manufacturer_name | |
| ndc | package | 59623-013-01 | openfda.package_ndc |
| ndc | package | 59623-013-02 | openfda.package_ndc |
| ndc | product | 59623-013 | openfda.product_ndc |
| ndc11 | package | 59623001302 | derived:openfda.package_ndc |
| ndc11 | package | 59623001301 | derived:openfda.package_ndc |
| spl id | 416205c4-4fec-1e12-e063-6294a90af417 | id | |
| spl set id | 067ee707-7219-4370-9cdd-08888f45b5e5 | set_id | |
| unii | 4K7Z7K7SWG | openfda.unii | |
| unii | 68OG1407SM | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | D1A2NG69CK | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | 5398RXP8KU | openfda.unii | |
| unii | 4D7G21HDBC | openfda.unii | |
| unii | HR6H5057CO | openfda.unii | |
| unii | 3LN5B70U4W | openfda.unii | |
| unii | TBW53313S7 | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | FEE198DK4Q | openfda.unii | |
| unii | 52B29REC7H | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | 9IOA40ANG6 | openfda.unii | |
| unii | X88DF51T48 | 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.