warnings
Warnings Do not use: to treat food allergies for persistent or chronic cough for treating cough from asthma, smoking, or emphysema for treating cough with excessive mucus A persistent cough may be a sign of a serious condition Warnings
Dr. Talbots Infant Daily Allergy 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 Daily Allergy Relief
- Generic name
- ALLIUM CEPA, ARALIA RACEMOSA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, LUFFA OPERCULATA, PULSATILLA, SOLIDAGO, NATRUM MURIATICUM
- Manufacturer
- Talbot's Pharmaceuticals Family Products, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c0963200-67dd-6349-e053-2a95a90adde1
- SPL ID
- c0963200-67de-6349-e053-2a95a90adde1
- Version
- 1
- Effective date
- 2021-04-22
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:30
| 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 Daily Allergy Relief | openfda.brand_name | |
| generic name | ALLIUM CEPA, ARALIA RACEMOSA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, LUFFA OPERCULATA, PULSATILLA, SOLIDAGO, NATRUM MURIATICUM | openfda.generic_name | |
| manufacturer name | Talbot's Pharmaceuticals Family Products, LLC | openfda.manufacturer_name | |
| ndc | package | 70797-308-04 | openfda.package_ndc |
| ndc | package | 70797-308-01 | openfda.package_ndc |
| ndc | product | 70797-308 | openfda.product_ndc |
| ndc11 | package | 70797030801 | derived:openfda.package_ndc |
| ndc11 | package | 70797030804 | derived:openfda.package_ndc |
| spl id | c0963200-67de-6349-e053-2a95a90adde1 | id | |
| spl set id | c0963200-67dd-6349-e053-2a95a90adde1 | set_id | |
| unii | C9642I91WL | openfda.unii | |
| unii | 3POA0Q644U | openfda.unii | |
| unii | 93PH5Q8M7E | openfda.unii | |
| unii | T90W4582DU | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | C4MO6809HU | openfda.unii | |
| unii | 492225Q21H | openfda.unii | |
| unii | 5405K23S50 | openfda.unii | |
| unii | I76KB35JEV | 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.