warnings
WARNINGS Warnings: Stop use and ask doctor if: fever wosens or lasts more than 2 days pain gets worse or lasts more than 7 days other symptoms persist for more than 7 days or worsen Warnings
Dr Talbots Infant Pain Fever 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 Fever Relief
- Generic name
- CALENDULA OFFICINALIS 12X,CHAMOMILLA 12X,ECHINACEA ANGUSTIFOLIA 12X,EUPATORIUM PERFOLIATUM 12X,HEPAR SULPHURIS CALCAREUM 12X,SULPHUR 12X,FERRUM PHOSPHORICUM 12X,KALI MURIATICUM 6X
- Manufacturer
- Talbot's Pharmaceuticals Family Products,LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e881a3ce-8cf9-0ce6-e053-2995a90ae824
- SPL ID
- eff981fd-5437-7c34-e053-2a95a90a3e8e
- Version
- 2
- Effective date
- 2022-12-16
- 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 05:15:19
| 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 Fever Relief | openfda.brand_name | |
| generic name | CALENDULA OFFICINALIS 12X,CHAMOMILLA 12X,ECHINACEA ANGUSTIFOLIA 12X,EUPATORIUM PERFOLIATUM 12X,HEPAR SULPHURIS CALCAREUM 12X,SULPHUR 12X,FERRUM PHOSPHORICUM 12X,KALI MURIATICUM 6X | openfda.generic_name | |
| manufacturer name | Talbot's Pharmaceuticals Family Products,LLC. | openfda.manufacturer_name | |
| ndc | package | 70797-318-01 | openfda.package_ndc |
| ndc | product | 70797-318 | openfda.product_ndc |
| ndc11 | package | 70797031801 | derived:openfda.package_ndc |
| spl id | eff981fd-5437-7c34-e053-2a95a90a3e8e | id | |
| spl set id | e881a3ce-8cf9-0ce6-e053-2995a90ae824 | set_id | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | 91GQH8I5F7 | openfda.unii | |
| unii | VB06AV5US8 | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | 1W0775VX6E | openfda.unii | |
| unii | G0R4UBI2ZZ | openfda.unii | |
| unii | WKB165X336 | openfda.unii | |
| unii | 1MBW07J51Q | 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.