United States · FDA National Drug Code directory
Dr Talbots Infant Daily Allergy Relief
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70797-322_e8bdcc8a-c948-ff5d-e053-2a95a90a3b92
- Product NDC
- 70797-322
- Form
- LIQUID
- Composition / generic term
- Allium cepa 12X,Aralia racemosa 12X,Euphrasia officinalis 12X,Galphimia glauca 12X,Histaminum hydrochloricum 12X,Luffa operculata 12X,Pulsatilla 12X,Solidago 12X,Natrum muriaticum 6X
- Labeler
- Talbot's Pharmaceuticals Family Products,LLC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20220912
- Source listing expiry
- 20261231
Source-listed ingredients
- ARALIA RACEMOSA ROOT — 12 [hp_X]/118mL
- EUPHRASIA STRICTA — 12 [hp_X]/118mL
- LUFFA OPERCULATA FRUIT — 12 [hp_X]/118mL
- ONION — 12 [hp_X]/118mL
- ANEMONE PULSATILLA — 12 [hp_X]/118mL
- HISTAMINE DIHYDROCHLORIDE — 12 [hp_X]/118mL
- SOLIDAGO VIRGAUREA FLOWERING TOP — 12 [hp_X]/118mL
- GALPHIMIA GLAUCA FLOWERING TOP — 12 [hp_X]/118mL
- SODIUM CHLORIDE — 6 [hp_X]/118mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (70797-322-01) / 118 mL in 1 BOTTLE · 70797-322-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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