Kids Relief

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
Generic name: DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CHAMOMILLA, COFFEE CRUDEA
Manufacturer: Homeolab International (Canada) inc
Product type: HUMAN OTC DRUG
SPL set ID: cacffbb1-c872-46ea-add0-bc7261da32e7
SPL ID: 1cb513cf-ca7d-4501-845a-ae052103c866
Version: 3
Effective date: 2022-11-21
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:12:47

Harmonized routes table
Harmonized routes
ORAL

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Kids Relief	openfda.brand_name
generic name		DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CHAMOMILLA, COFFEE CRUDEA	openfda.generic_name
manufacturer name		Homeolab International (Canada) inc	openfda.manufacturer_name
ndc	package	71971-9151-4	openfda.package_ndc
ndc	package	71971-9151-5	openfda.package_ndc
ndc	package	71971-9151-9	openfda.package_ndc
ndc	product	71971-9151	openfda.product_ndc
ndc11	package	71971915104	derived:openfda.package_ndc
ndc11	package	71971915109	derived:openfda.package_ndc
ndc11	package	71971915105	derived:openfda.package_ndc
spl id		1cb513cf-ca7d-4501-845a-ae052103c866	id
spl set id		cacffbb1-c872-46ea-add0-bc7261da32e7	set_id
unii		387GMG9FH5	openfda.unii
unii		3SW678MX72	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		LZB7TFX1LT	openfda.unii
unii		BJ7YPN79A1	openfda.unii
unii		75O014T1HG	openfda.unii
unii		FGL3685T2X	openfda.unii
unii		22Z32PWR7R	openfda.unii
unii		56K0VVT47P	openfda.unii

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 i f •pain or cough gets worse or lasts 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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.