kids cough

Manufacturer
Natures Investment Holdings Pty Ltd dba Maxrelief USA | KEYSUN PTY. LIMITED Also Traded as KEYSUN LABORATORIES
Effective date
2014-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:05:44

Label at a glance#

Productkids cough
Active ingredientDROSERA INTERMEDIA, SPONGIA OFFICINALIS WHOLE, POTASSIUM CARBONATE, PHOSPHORUS, PULSATILLA VULGARIS, ATROPA BELLADONNA, IPECAC
Label structure9 sections

Storage and handling

STORE BELOW 30 C

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Non-Active Ingredients

Isomalt, Natural Raspberry Flavour and Natural Colour Carmine E120 (Cochineal)

OTC - ACTIVE INGREDIENT SECTION

Each lozenge contains:

Drosera 30C, Spongia 30C,

Kali Carbonicum 30C,

Phospherous 30C, Ipeacacuanha 30C,

Pulsatilla 30C, Belladonna 30C

in equal quantities.

OTC - PURPOSE SECTION

Indications

For natural, temporary relief of

cough and sore throat symptoms

(hoarseness and dry cough)

WARNINGS SECTION

Warning: If symptoms persist or worsen suddenly, consult your

healthcare specialist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all other medicines out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

For best results, begin taking one

KidsCough at the first sign of a cough or sore throat.

Suck KidsCough and avoid chewing as it reduces

absorption of active ingredients. Recommended dosage

3 per day. Use only when symptoms exist. Not to be used

in children under 2 years of age without medical advice.

INDICATIONS & USAGE SECTION

Indications

For natural, temporary relief of

cough and sore throat symptoms

(hoarseness and dry cough). If

coughing persists, consult a healthcare professional.

STORAGE AND HANDLING SECTION

STORE BELOW 30 C

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

copy of labelcopy of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76509-180-012019-11-27C16284748780-19855e2a2-386d-60a7-e053-dbdaa90a05bdHomeopathic Drug Facts
76509-180-022019-11-27C16284748780-19855e2a2-386d-60a7-e053-dbdaa90a05bdHomeopathic Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76509-180-01kids cough10 in 1 BOXLOZENGE101
76509-180-02kids cough10 in 1 BOXLOZENGE101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76509-180KIDS COUGH (DROSERA 30C, SPONGIA 30C, KALI CARBONICUM 30C, PHOSPHEROUS 30C, IPEACACUHUANA 30C, PULSATILLA 30C, BELLADONNA 30C) LOZENGE [NATURES INVESTMENT HOLDINGS PTY LTD DBA MAXRELIEF USA]1Legacy NDC, 2 package rows20140513_fac70d3b-b2d9-4dc4-a03e-e6c128dc4672.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0H1
DROSERA INTERMEDIAACTIVE INGREDIENTB3G4A96QLY1
IPECACACTIVE INGREDIENT62I3C8233L1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
POTASSIUM CARBONATEACTIVE INGREDIENTBQN1B9B9HA1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
SPONGIA OFFICINALIS WHOLEACTIVE INGREDIENT755U7L3M7Z1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0H1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7D1
DROSERA INTERMEDIAACTIVE MOIETYB3G4A96QLY1
IPECACACTIVE MOIETY62I3C8233L1
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
SPONGIA OFFICINALIS WHOLEACTIVE MOIETY755U7L3M7Z1
COCHINEALINACTIVE INGREDIENTTZ8Z31B35M1
ISOMALTINACTIVE INGREDIENTS870P55O2W1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76509-18076509-180-01, 76509-180-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 5 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOMALTISOMALTS870P55O2WTROCHE / ORAL1718.71 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WTABLET, CHEWABLE / ORAL630 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WPOWDER / SUBLINGUAL530 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WTABLET / ORAL522 mgExact identifier — unii candidate
5 equally ranked IID candidates
ISOMALTISOMALTS870P55O2WCAPSULE / ORAL158 mgExact identifier — unii candidate
5 equally ranked IID candidates

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4ff88769-7699-42c4-ac40-86fc9c6b441efac70d3b-b2d9-4dc4-a03e-e6c128dc46722014-05-13WarningsExact identifier
spl id: 4ff88769-7699-42c4-ac40-86fc9c6b441e
spl set id: fac70d3b-b2d9-4dc4-a03e-e6c128dc4672

Reported adverse events (FAERS/openFDA)#

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