warnings
WARNING: IF PREGNANT OR BREAST FEEDING, ask a health professional before use. If symptoms worsen or persist, discontinue use and consult with your doctor. KEEP OUT OF REACH OF CHILDREN.
OHM Mucus Relief
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
- OHM Mucus Relief
- Generic name
- ANTIMONIUM CRUDUM, ANTIMONIUM TARTARICUM, CHELIDONIUM MAJUS, FERRUM PHOSPHORICUM, KALI CARBOONICUM, KALI MURIATICUM, KALI SULPHURICUM, MARRUBIUM VULGARE.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f13bff50-7087-46dc-a958-b460a2af6283
- SPL ID
- b8a719c7-3b71-773b-e053-2995a90af29b
- Version
- 3
- Effective date
- 2021-01-11
- Source export date
- 2026-10-27
- 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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:15:28
| 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 | OHM Mucus Relief | openfda.brand_name | |
| generic name | ANTIMONIUM CRUDUM, ANTIMONIUM TARTARICUM, CHELIDONIUM MAJUS, FERRUM PHOSPHORICUM, KALI CARBOONICUM, KALI MURIATICUM, KALI SULPHURICUM, MARRUBIUM VULGARE. | openfda.generic_name | |
| manufacturer name | OHM PHARMA INC. | openfda.manufacturer_name | |
| ndc | package | 66096-706-23 | openfda.package_ndc |
| ndc | product | 66096-706 | openfda.product_ndc |
| ndc11 | package | 66096070623 | derived:openfda.package_ndc |
| spl id | b8a719c7-3b71-773b-e053-2995a90af29b | id | |
| spl set id | f13bff50-7087-46dc-a958-b460a2af6283 | set_id | |
| unii | 7E889U5RNN | openfda.unii | |
| unii | F79059A38U | openfda.unii | |
| unii | DL6OZ476V3 | openfda.unii | |
| unii | BQN1B9B9HA | openfda.unii | |
| unii | 91GQH8I5F7 | openfda.unii | |
| unii | 1K573LC5TV | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | 7A72MUN24Z | openfda.unii | |
| unii | T4423S18FM | 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.