Home NDC 71971-9066 Kids Relief
Product NDC 71971-9066
11-digit product format 719719066
Labeler code 71971
Product ID 71971-9066_27e95caf-7afc-437c-b7c0-05f6df793fbc
Type HUMAN OTC DRUG
Nonproprietary name PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, ARALIA RACEMOSA, CUPRUM METALLICUM
Dosage form LIQUID
Route ORAL
Labeler Homeolab International (Canada) inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-07-26
Substance ANEMONE PULSATILLA; ONION; ARSENIC TRIOXIDE; STRYCHNOS NUX-VOMICA SEED; EUPHRASIA STRICTA; SCHOENOCAULON OFFICINALE SEED; ARALIA RACEMOSA ROOT; COPPER
Active strength 8; 6; 8; 6; 6; 6; 6; 8 [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL
Pharmacologic classes Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Kids Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength 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 ARALIA RACEMOSA ROOT 6 [hp_X]/25mL COPPER 8 [hp_X]/25mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71971-9066-8 Kids Relief 25 mL in 1 BOTTLE LIQUID 25 1 71971-9066-8 Kids Relief 1 in 1 CARTON LIQUID 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71971-9066 KIDS RELIEF (PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, ARALIA RACEMOSA, CUPRUM METALLICUM) LIQUID [HOMEOLAB INTERNATIONAL (CANADA) INC] 1 Current NDC, Legacy NDC, 2 package rows 20190801_7978fb75-fac9-480d-830c-c8c09ff29be1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kids Relief PULSATILLA, ALLIUM CEPA, ARSENICUM ALBUM, NUX VOMICA, EUPHRASIA OFFINALIS, SABADILLA, ARALIA RACEMOSA, CUPRUM METALLICUM Homeolab International (Canada) inc 7978fb75-fac9-480d-830c-c8c09ff29be1 2019-07-25 Warnings Exact identifier ndc (product): 71971-9066
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71971-9066-8 71971906608 1 BOTTLE in 1 CARTON (71971-9066-8) / 25 mL in 1 BOTTLE 1 bottle 2019-07-26 0000-00-00 No No Current