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: Laboratoire Atlas Inc
Product type: HUMAN OTC DRUG
SPL set ID: de020891-eca2-405c-81cd-75dfb4ffe586
SPL ID: 40aacaf1-ccd0-3ffb-e063-6394a90aa4df
Version: 8
Effective date: 2025-10-08
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:07

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		Laboratoire Atlas Inc	openfda.manufacturer_name
ndc	package	63388-915-19	openfda.package_ndc
ndc	package	63388-915-14	openfda.package_ndc
ndc	package	63388-915-15	openfda.package_ndc
ndc	product	63388-915	openfda.product_ndc
ndc11	package	63388091514	derived:openfda.package_ndc
ndc11	package	63388091519	derived:openfda.package_ndc
ndc11	package	63388091515	derived:openfda.package_ndc
spl id		40aacaf1-ccd0-3ffb-e063-6394a90aa4df	id
spl set id		de020891-eca2-405c-81cd-75dfb4ffe586	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.