United States · FDA National Drug Code directory

Dr. Talbots 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: 70797-312_cda1180e-7f6a-69b2-e053-2995a90a5015
Product NDC: 70797-312
Form: LIQUID
Composition / generic term: Allium cepa, Aralia racemosa, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Luffa operculata, Pulsatilla, Solidago, Natrum muriaticum
Labeler: Talbot's Pharmaceuticals Family Products, LLC.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20200720
Source listing expiry: 20261231

Source-listed ingredients

ARALIA RACEMOSA ROOT — 12 [hp_X]/118mL
GALPHIMIA GLAUCA FLOWERING TOP — 12 [hp_X]/118mL
LUFFA OPERCULATA FRUIT — 12 [hp_X]/118mL
EUPHRASIA STRICTA — 12 [hp_X]/118mL
HISTAMINE DIHYDROCHLORIDE — 12 [hp_X]/118mL
ANEMONE PULSATILLA — 12 [hp_X]/118mL
ONION — 12 [hp_X]/118mL
SODIUM CHLORIDE — 6 [hp_X]/118mL
SOLIDAGO VIRGAUREA FLOWERING TOP — 12 [hp_X]/118mL

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (70797-312-01) / 118 mL in 1 BOTTLE (70797-312-04) · 70797-312-01

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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