warnings
Warning Warnings: Stop use and ask doctor if: fever develops diarrhea lasts more than 2 days other symtomps persist for more than 7 days or worse
Dr Talbots Infant Tummy Ache 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 Tummy Ache Relief
- Generic name
- CALENDULA OFFICINALIS 12X,CARBO VEGETABILIS 12X,LYCOPODIUM 30X,FOENICULUM VULGARE 12X,NUX MOSCHATA 12X,ZINGIBER OFFICINALE 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 12X,NATRUM PHOSPHORICUM 6X
- Manufacturer
- Talbot's Pharmaceuticals Family Products,LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e9c24994-b935-36e6-e053-2a95a90a78df
- SPL ID
- e9c24994-b936-36e6-e053-2a95a90a78df
- Version
- 1
- Effective date
- 2022-09-28
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:17
| 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 Tummy Ache Relief | openfda.brand_name | |
| generic name | CALENDULA OFFICINALIS 12X,CARBO VEGETABILIS 12X,LYCOPODIUM 30X,FOENICULUM VULGARE 12X,NUX MOSCHATA 12X,ZINGIBER OFFICINALE 12X,KALI MURIATICUM 6X,MAGNESIA PHOSPHORICA 12X,NATRUM PHOSPHORICUM 6X | openfda.generic_name | |
| manufacturer name | Talbot's Pharmaceuticals Family Products,LLC. | openfda.manufacturer_name | |
| ndc | package | 70797-317-01 | openfda.package_ndc |
| ndc | product | 70797-317 | openfda.product_ndc |
| ndc11 | package | 70797031701 | derived:openfda.package_ndc |
| spl id | e9c24994-b936-36e6-e053-2a95a90a78df | id | |
| spl set id | e9c24994-b935-36e6-e053-2a95a90a78df | set_id | |
| unii | 2P3VWU3H10 | openfda.unii | |
| unii | 18E7415PXQ | openfda.unii | |
| unii | AEE24M3MQ9 | openfda.unii | |
| unii | G3QC02NIE6 | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 660YQ98I10 | openfda.unii | |
| unii | G0R4UBI2ZZ | openfda.unii | |
| unii | C5529G5JPQ | openfda.unii | |
| unii | 70WT22SF4B | openfda.unii | |
| unii | C88X29Y479 | 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.