United States · FDA National Drug Code directory

Pertussis

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
43742-1089_a1ee91c3-0ca9-4129-9e5d-aa26669f24bf
Product NDC
43742-1089
Form
LIQUID
Composition / generic term
Aconitum Napellus, Bryonia (Alba), Hyoscyamus Niger, Ipecacuanha, Sticta Pulmonaria, Tabacum, Phosphorus, Antimonium Tartaricum, Kreosotum, Silicea, Pertussinum, Tetanus Toxin
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20171031
Source listing expiry
20261231

Source-listed ingredients

  • ACONITUM NAPELLUS — 4 [hp_X]/mL
  • BRYONIA ALBA ROOT — 4 [hp_X]/mL
  • HYOSCYAMUS NIGER — 4 [hp_X]/mL
  • IPECAC — 4 [hp_X]/mL
  • LOBARIA PULMONARIA — 4 [hp_X]/mL
  • TOBACCO LEAF — 4 [hp_X]/mL
  • PHOSPHORUS — 5 [hp_X]/mL
  • ANTIMONY POTASSIUM TARTRATE — 6 [hp_X]/mL
  • WOOD CREOSOTE — 6 [hp_X]/mL
  • SILICON DIOXIDE — 8 [hp_X]/mL
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED — 30 [hp_X]/mL
  • CLOSTRIDIUM TETANI — 30 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 mL in 1 BOTTLE, DROPPER (43742-1089-1) · 43742-1089-1

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 →