FDA.reportPublic FDA data

Kids Relief

Manufacturer
Homeolab International (Canada) inc
Effective date
2022-11-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:19:09

Label at a glance#

ProductKids Relief
Active ingredientDROSERA ROTUNDIFOLIA FLOWERING TOP, ARNICA MONTANA, BRYONIA ALBA WHOLE, CETRARIA ISLANDICA SUBSP. ISLANDICA, PROTORTONIA CACTI, TIN, CHAMOMILE, ARABICA COFFEE BEAN, CORALLIUM RUBRUM WHOLE
Label structure9 sections

Storage and handling

Other information •Store at room temperature. •Do not use if seal is broken or missing.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients HPUS

Drosera 1C

Arnica Montana 3C

Bryonia 3C

Cetraria islandica 3C

Coccus cacti 3C

Corallium rubrum 3C

Stannum metallicum 3C

Chamomilla 4C

Coffee crudea 4C

OTC - PURPOSE SECTION

Purpose

Drosera 1C...........................dry cough

Arnica Montana 3C.................aches and pains, chest congestion

Bryonia 3C............................painful cough

Cetraria islandica 3C...............cough with expectoration

Coccus cacti 3C......................cough with expectoration

Corallium rubrum 3C...............painful cough

Stannum metallicum 3C...........cough, chills and lessens mucus

Chamomilla 4C.......................restlessness, irritability, nocturnal awakenings

Coffee crudea 4C....................restlessness and sleeplessness

The letters "HPUS" indicate that the components in this product are officially

monographed in the Homeopathic Pharmacopoeia of the United States

INDICATIONS & USAGE SECTION

Uses This homeopathic medicine is made from a combination

of ingredients traditionally used to help relieve 

symptoms associated with nighttime cough and cold:

•dry cough  •cough with expectoration  

•chest congestion  •fever  •aches and pains

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental

overdose, contact a medical professional or a poison

control center immediately. 

DOSAGE & ADMINISTRATION SECTION

Directions •Chidren under 6 months of age: Consult

a licensed healthcare professional before using this product

•Children 6 months to 2 years old: 2.5ml or 1/2 teaspoon,

every 8 hours or 3 times a day •Children 2 to 12 years

old: 5ml or 1 teaspoon, every 8 hours or 3 times a day. 

STORAGE AND HANDLING SECTION

Other information •Store at room temperature.

•Do not use if seal is broken or missing.

INACTIVE INGREDIENT SECTION

Inactive ingredients Purified water, sorbitol,

caramel, sodium benzoate, potassium sorbate, citric acid

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71971-9151-4Kids Relief30 mL in 1 BOTTLELIQUID303
71971-9151-5Kids Relief100 mL in 1 BOTTLELIQUID1003
71971-9151-5Kids Relief1 in 1 CARTONLIQUID13
71971-9151-9Kids Relief250 mL in 1 BOTTLELIQUID2503
71971-9151-9Kids Relief1 in 1 CARTONLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71971-9151KIDS RELIEF (DROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CHAMOMILLA, COFFEE CRUDEA) LIQUID [HOMEOLAB INTERNATIONAL (CANADA) INC]3Current NDC, Legacy NDC, 5 package rows20221229_cacffbb1-c872-46ea-add0-bc7261da32e7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71971-915171971-9151-5, 71971-9151-9, 71971-9151-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
DROSERA ROTUNDIFOLIA FLOWERING TOP75O014T1HGACTIB
ARNICA MONTANAO80TY208ZWACTIB
BRYONIA ALBA WHOLE56K0VVT47PACTIB
CETRARIA ISLANDICA SUBSP. ISLANDICABJ7YPN79A1ACTIB
PROTORTONIA CACTILZB7TFX1LTACTIB
TIN387GMG9FH5ACTIB
CHAMOMILEFGL3685T2XACTIB
ARABICA COFFEE BEAN3SW678MX72ACTIB
WATER059QF0KO0RIACT
SORBITOL506T60A25RIACT
CARAMELT9D99G2B1RIACT
SODIUM BENZOATEOJ245FE5EUIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
CORALLIUM RUBRUM WHOLE22Z32PWR7RACTIB

Source Document#

Source XML

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Kids Relief Cough and Cold Syrup Combo Pack Daytime Formula and Nighttime FormulaDROSERA ROTUNDIFOLIA FLOWERING TOP, ARNICA MONTANA, BRYONIA ALBA WHOLE, IPECACUANHA, CETRARIA ISLANDICA SUBSP. ISLANDICA, COCHINEAL, CORALLIUM RUBRUM WHOLE, STANNUM METALLICUM, CHAMOMILLA, COFFEA CRUDAHomeolab International (Canada) incab37b0fd-cd18-4823-baef-dedadac862362025-07-30WarningsExact identifier
ndc (package): 71971-9151-5
ndc11 (package): 71971915105
Kids ReliefDROSERA, ARNICA MONTANA, BRYONIA, CETRARIA ISLANDICA, COCCUS CACTI, CORALLIUM RUBRUM, STANNUM METALLICUM, CHAMOMILLA, COFFEE CRUDEAHomeolab International (Canada) inccacffbb1-c872-46ea-add0-bc7261da32e72022-11-21WarningsExact identifier
ndc (package): 71971-9151-4
ndc (package): 71971-9151-5
ndc (package): 71971-9151-9
ndc (product): 71971-9151
ndc11 (package): 71971915104
ndc11 (package): 71971915109
ndc11 (package): 71971915105
spl id: 1cb513cf-ca7d-4501-845a-ae052103c866
spl set id: cacffbb1-c872-46ea-add0-bc7261da32e7

Reported adverse events (FAERS/openFDA)#

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