United States · FDA National Drug Code directory

Dr. Talbots Mucus Cold 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
70797-313_cda11a45-601a-dbac-e053-2a95a90a2c1b
Product NDC
70797-313
Form
LIQUID
Composition / generic term
Eupatorium perf, Hepar sulphuris calcareum, Kali bichromicum, Marrubium vulgare, Phosphorus, Pulsatilla, Rumex crispus, Sambucus nigra, Calcarea sulphurica, Ferrum phosphoricum, Kali 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

  • EUPATORIUM PERFOLIATUM FLOWERING TOP — 12 [hp_X]/118mL
  • SAMBUCUS NIGRA FLOWERING TOP — 12 [hp_X]/118mL
  • CALCIUM SULFATE ANHYDROUS — 12 [hp_X]/118mL
  • POTASSIUM CHLORIDE — 6 [hp_X]/118mL
  • MARRUBIUM VULGARE — 12 [hp_X]/118mL
  • PHOSPHORUS — 30 [hp_X]/118mL
  • RUMEX CRISPUS ROOT — 12 [hp_X]/118mL
  • FERROSOFERRIC PHOSPHATE — 12 [hp_X]/118mL
  • CALCIUM SULFIDE — 12 [hp_X]/118mL
  • POTASSIUM DICHROMATE — 12 [hp_X]/118mL
  • ANEMONE PULSATILLA — 12 [hp_X]/118mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (70797-313-01) / 118 mL in 1 BOTTLE (70797-313-04) · 70797-313-01

Source and coverage

Open FDA National Drug Code directory →

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.

Browse United States records →