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, IPECACUANHA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM
Manufacturer: Laboratoire Atlas Inc
Product type: HUMAN OTC DRUG
SPL set ID: fbce712e-3073-4afd-adfe-19fb55c6689b
SPL ID: 40aac810-8f25-985a-e063-6394a90a5583
Version: 5
Effective date: 2025-10-08
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:58:44

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Kids Relief	openfda.brand_name
generic name		DROSERA, ARNICA MONTANA, BRYONIA, IPECACUANHA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM	openfda.generic_name
manufacturer name		Laboratoire Atlas Inc	openfda.manufacturer_name
ndc	package	63388-912-15	openfda.package_ndc
ndc	package	63388-912-14	openfda.package_ndc
ndc	package	63388-912-19	openfda.package_ndc
ndc	product	63388-912	openfda.product_ndc
ndc11	package	63388091214	derived:openfda.package_ndc
ndc11	package	63388091219	derived:openfda.package_ndc
ndc11	package	63388091215	derived:openfda.package_ndc
spl id		40aac810-8f25-985a-e063-6394a90a5583	id
spl set id		fbce712e-3073-4afd-adfe-19fb55c6689b	set_id
unii		387GMG9FH5	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		BJ7YPN79A1	openfda.unii
unii		75O014T1HG	openfda.unii
unii		62I3C8233L	openfda.unii
unii		22Z32PWR7R	openfda.unii
unii		56K0VVT47P	openfda.unii
unii		TZ8Z31B35M	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 if •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.