Home FDA labels 3b271a2a-f5ea-5d80-e063-6394a90a9282 Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula
Generic name DROSERA ROTUNDIFOLIA FLOWERING TOP, ARNICA MONTANA, BRYONIA ALBA WHOLE, IPECACUANHA, CETRARIA ISLANDICA SUBSP. ISLANDICA, COCHINEAL, CORALLIUM RUBRUM WHOLE, STANNUM METALLICUM, CHAMOMILLA, COFFEA CRUDA
Manufacturer Homeolab International (Canada) inc
Product type HUMAN OTC DRUG
SPL set ID ab37b0fd-cd18-4823-baef-dedadac86236
SPL ID 3b271a2a-f5ea-5d80-e063-6394a90a9282
Version 2
Effective date 2025-07-30
Source export date 2026-09-28
Source partition 1
Source file https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:12:39 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 12 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime Formula openfda.brand_name generic name DROSERA ROTUNDIFOLIA FLOWERING TOP, ARNICA MONTANA, BRYONIA ALBA WHOLE, IPECACUANHA, CETRARIA ISLANDICA SUBSP. ISLANDICA, COCHINEAL, CORALLIUM RUBRUM WHOLE, STANNUM METALLICUM, CHAMOMILLA, COFFEA CRUDA openfda.generic_name manufacturer name Homeolab International (Canada) inc openfda.manufacturer_name ndc package 71971-9151-5 openfda.package_ndc ndc package 71971-6105-7 openfda.package_ndc ndc package 71971-9121-5 openfda.package_ndc ndc product 71971-6105 openfda.product_ndc ndc11 package 71971610507 derived:openfda.package_ndc ndc11 package 71971915105 derived:openfda.package_ndc ndc11 package 71971912105 derived:openfda.package_ndc spl id 3b271a2a-f5ea-5d80-e063-6394a90a9282 id spl set id ab37b0fd-cd18-4823-baef-dedadac86236 set_id
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings Stop use and ask a doctor if: • Pain & cough get worse or last more than 5 days (children) or 7 days (adults). • Fever gets worse or lasts more than 3 days. • Redness or swelling is present. • New symptoms occur. • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition. Keep out of reach of children. In case of accidental overdose, contact a medical professional or poison control center immediately.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.