warnings
WARNINGS: IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor. KEEP OUT OF THE REACH OF CHILDREN.
OHM Mouthwash
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 Mouthwash
- Generic name
- ARNICA MONTANA, BORAX, CALENDULA OFFICINALIS, HYPERICUM PERFORATUM, MYRRHA, PLANTAGO MAJOR, RATANHIA, SALVIA OFFICINALIS, SYMPHYTUM OFFICINALE.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 4fa493ff-9ea2-4e17-9e16-994c11207440
- SPL ID
- d44b4ca0-1534-446b-e053-2a95a90a32e6
- Version
- 4
- Effective date
- 2021-12-29
- Source export date
- 2026-10-30
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:11:11
| 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 Mouthwash | openfda.brand_name | |
| generic name | ARNICA MONTANA, BORAX, CALENDULA OFFICINALIS, HYPERICUM PERFORATUM, MYRRHA, PLANTAGO MAJOR, RATANHIA, SALVIA OFFICINALIS, SYMPHYTUM OFFICINALE. | openfda.generic_name | |
| manufacturer name | OHM PHARMA INC. | openfda.manufacturer_name | |
| ndc | package | 66096-159-05 | openfda.package_ndc |
| ndc | product | 66096-159 | openfda.product_ndc |
| ndc11 | package | 66096015905 | derived:openfda.package_ndc |
| spl id | d44b4ca0-1534-446b-e053-2a95a90a32e6 | id | |
| spl set id | 4fa493ff-9ea2-4e17-9e16-994c11207440 | set_id | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | 91MBZ8H3QO | openfda.unii | |
| unii | M9VVZ08EKQ | openfda.unii | |
| unii | W2469WNO6U | openfda.unii | |
| unii | P29ZH1A35Z | openfda.unii | |
| unii | 065C5D077J | openfda.unii | |
| unii | JC71GJ1F3L | 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.