warnings
Warnings Warnings Do not use: for persistent or chronic cough for treating cough from asthama, smoking, or emphysema for treating cough with excessive mucus A persistent cough may be a sign of a serious condition Warning
Dr Talbots Infant Cough 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 Cough Relief
- Generic name
- ANTIMONIUM TARTARICUM 12X,DROSERA ROTUNDIFOLIA 12X,IPECACUANHA 12X,PHOSPHORUS 12X,RUMEX CRISPUS 12X,SPONGIA TOSTA 12X,STICTA PULMONARIA 12X,KALI SULPHURICUM 6X
- Manufacturer
- Talbots Pharmaceuticals Family Products, LLC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e8902c05-3303-2e0f-e053-2a95a90aa15d
- SPL ID
- e8902c05-3304-2e0f-e053-2a95a90aa15d
- Version
- 1
- Effective date
- 2022-09-12
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:48:46
| 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 Cough Relief | openfda.brand_name | |
| generic name | ANTIMONIUM TARTARICUM 12X,DROSERA ROTUNDIFOLIA 12X,IPECACUANHA 12X,PHOSPHORUS 12X,RUMEX CRISPUS 12X,SPONGIA TOSTA 12X,STICTA PULMONARIA 12X,KALI SULPHURICUM 6X | openfda.generic_name | |
| manufacturer name | Talbots Pharmaceuticals Family Products, LLC. | openfda.manufacturer_name | |
| ndc | package | 70797-319-01 | openfda.package_ndc |
| ndc | product | 70797-319 | openfda.product_ndc |
| ndc11 | package | 70797031901 | derived:openfda.package_ndc |
| spl id | e8902c05-3304-2e0f-e053-2a95a90aa15d | id | |
| spl set id | e8902c05-3303-2e0f-e053-2a95a90aa15d | set_id | |
| unii | 27YLU75U4W | openfda.unii | |
| unii | CQN5KB2U1M | openfda.unii | |
| unii | 483B0A2Y00 | openfda.unii | |
| unii | 9N1RM2S62C | openfda.unii | |
| unii | 75O014T1HG | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | 1PIP394IID | 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.