United States · FDA National Drug Code directory

Respiforce B-HP

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
43857-0623_a712f2c0-c148-43a9-a7e6-fb6862968f30
Product NDC
43857-0623
Form
LIQUID
Composition / generic term
Carbo Vegetabilis, Cuprum Metallicum, Drosera (Rotundifolia), Ipecacuanha, Lachesis Mutus, Lobelia Inflata, Phosphorus, Pulsatilla (Vulgaris), Rumex Crispus, Spongia Tosta
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20220302
Source listing expiry
20261231

Source-listed ingredients

  • ACTIVATED CHARCOAL — 30 [hp_X]/mL
  • COPPER — 30 [hp_X]/mL
  • DROSERA ROTUNDIFOLIA WHOLE — 30 [hp_X]/mL
  • IPECAC — 30 [hp_X]/mL
  • LACHESIS MUTA VENOM — 30 [hp_X]/mL
  • LOBELIA INFLATA WHOLE — 30 [hp_X]/mL
  • PHOSPHORUS — 30 [hp_X]/mL
  • PULSATILLA VULGARIS WHOLE — 30 [hp_X]/mL
  • RUMEX CRISPUS ROOT — 30 [hp_X]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED — 30 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 mL in 1 BOTTLE, DROPPER (43857-0623-1) · 43857-0623-1

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 →