warnings
Warning Warnings: Stop use and ask a doctor if: fever develops, worsens, or lasts more than 3 days pain gets worse or lasts more than 7 days other symtoms persist for more than 7 days or worsen
Dr Talbots Infant Pain Inflamtion 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
- Dr Talbots Infant Pain Inflamtion Relief
- Generic name
- ARNICA 12X,BELLIS PERENNIS 12X,CALENDULA OFFICINALIS 12X,CHAMOMILLA 12X,COFFEA CRUDA 12X,HYPERICUM 12X,MILLEFOLIUM 12X,FERRUM PHOSPHORICUM 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 6X
- Manufacturer
- Talbots Pharmaceuticals Family Products, LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e892c0cb-03b4-52da-e053-2995a90a0878
- SPL ID
- e892c0cb-03b5-52da-e053-2995a90a0878
- Version
- 1
- Effective date
- 2022-09-12
- Source export date
- 2026-10-27
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:09:44
| 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 | Dr Talbots Infant Pain Inflamtion Relief | openfda.brand_name | |
| generic name | ARNICA 12X,BELLIS PERENNIS 12X,CALENDULA OFFICINALIS 12X,CHAMOMILLA 12X,COFFEA CRUDA 12X,HYPERICUM 12X,MILLEFOLIUM 12X,FERRUM PHOSPHORICUM 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 6X | openfda.generic_name | |
| manufacturer name | Talbots Pharmaceuticals Family Products, LLC. | openfda.manufacturer_name | |
| ndc | package | 70797-321-01 | openfda.package_ndc |
| ndc | product | 70797-321 | openfda.product_ndc |
| ndc11 | package | 70797032101 | derived:openfda.package_ndc |
| spl id | e892c0cb-03b5-52da-e053-2995a90a0878 | id | |
| spl set id | e892c0cb-03b4-52da-e053-2995a90a0878 | set_id | |
| unii | XK4IUX8MNB | openfda.unii | |
| unii | 3SW678MX72 | openfda.unii | |
| unii | O80TY208ZW | openfda.unii | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | 2HU33I03UY | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 91GQH8I5F7 | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | G0R4UBI2ZZ | 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.