United States · FDA National Drug Code directory

Kids 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
71971-9077_89e04889-f92f-41d0-9e45-a5eddb46453f
Product NDC
71971-9077
Form
LIQUID
Composition / generic term
PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, STICTA PULMONARIA, ARAILA RACEMOSA, CUPRUM METALLICUM
Labeler
Homeolab International (Canada) inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20170303
Source listing expiry
20261231

Source-listed ingredients

  • ANEMONE PULSATILLA — 8 [hp_X]/25mL
  • ONION — 6 [hp_X]/25mL
  • ARSENIC TRIOXIDE — 8 [hp_X]/25mL
  • STRYCHNOS NUX-VOMICA SEED — 6 [hp_X]/25mL
  • EUPHRASIA STRICTA — 6 [hp_X]/25mL
  • SCHOENOCAULON OFFICINALE SEED — 6 [hp_X]/25mL
  • LOBARIA PULMONARIA — 6 [hp_X]/25mL
  • ARALIA RACEMOSA ROOT — 6 [hp_X]/25mL
  • COPPER — 8 [hp_X]/25mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (71971-9077-8) / 25 mL in 1 BOTTLE · 71971-9077-8

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 →