warnings
Warning Use of this product may cause methemoglobinemia, a serious condition that requires immediate treatment because it reduces the oxygen-carrying capacity of the blood. This can happen even if you have used this product before.
Ora YoGu 4X Medicated Tooth and Gum Pain Reliever
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
- Ora YoGu 4X Medicated Tooth and Gum Pain Reliever
- Generic name
- MEDICATED TOOTH AND GUM PAIN RELIEVER
- Manufacturer
- Kungpo Health Care & Herbal Center Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1f10a72f-0b49-41cb-92f9-b0160d7664de
- SPL ID
- fa8ae828-9f80-42f2-b23b-21d6c4bcb383
- Version
- 33048
- Effective date
- 2026-04-22
- 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 05:15:23
| Harmonized routes |
|---|
| TOPICAL |
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 |
|---|---|---|---|
| application number | M022 | openfda.application_number | |
| brand name | Ora YoGu 4X Medicated Tooth and Gum Pain Reliever | openfda.brand_name | |
| generic name | MEDICATED TOOTH AND GUM PAIN RELIEVER | openfda.generic_name | |
| manufacturer name | Kungpo Health Care & Herbal Center Inc | openfda.manufacturer_name | |
| ndc | package | 87351-761-10 | openfda.package_ndc |
| ndc | product | 87351-761 | openfda.product_ndc |
| ndc11 | package | 87351076110 | derived:openfda.package_ndc |
| spl id | fa8ae828-9f80-42f2-b23b-21d6c4bcb383 | id | |
| spl set id | 1f10a72f-0b49-41cb-92f9-b0160d7664de | set_id | |
| unii | U3RSY48JW5 | openfda.unii | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | F5UM2KM3W7 | openfda.unii | |
| unii | 86Q357L16B | 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.