Cough Relief

Manufacturer
King Bio Inc.
Effective date
2011-11-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:03:26

Label at a glance#

ProductCough Relief
Active ingredientACONITUM NAPELLUS, BROMINE, PROTORTONIA CACTI, CORALLIUM RUBRUM EXOSKELETON, COPPER, DROSERA ROTUNDIFOLIA, FERROSOFERRIC PHOSPHATE, CALCIUM SULFIDE, IODINE, POTASSIUM DICHROMATE, MEPHITIS MEPHITIS ANAL GLAND FLUID, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, SANGUINARIA CANADENSIS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, SULFUR
Label structure8 sections

Indications and uses

Uses for temporary relief of minor cough symptoms from the common cold or inhaled irritants: Dry or hoarse cough hacking, tickling or spasmodic cough croupy cough and throat irritation Reference image cough relief.jpg

Label contents#

Full prescribing information#

Inactive Ingredient

OTC - ACTIVE INGREDIENT SECTION

Official HPUS: Aconitum Napellus, Bromium, Coccus Cacti, Corallium Rubrum, Cuprum Metallicum, Drosera Rotundifolia, Ferrum Phosphoricum, Hepar Sulphuris Calcareum, Iodium, Kali Bichromicum, Mephitis Mephitica, Nux Vomica, Phosphorus, Pulsatilla, Rumex Crispus, Sanguinaria Canadensis, Spongia Tosta and Sulphur.

Reference image cough relief.jpg

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Equal volumes of each ingredient in a Bio-Energetically Enhanced pure water base: 10X, 30X, and LM1 potencies.

Reference image cough relief.jpg

Purpose

OTC - PURPOSE SECTION

Uses for temporary relief of minor cough symptoms from the common cold or inhaled irritants: dry or hoarse cough, Hacking, tickling or spasmodic cough, croupy cough and throat irritation.

Note A persistent cough may be a sign of a serious condition. If cough is accompanied by fever, rash, persistent headache or breathing difficulties, consult a health care professional.

Reference image cough relief.jpg

Dosage

DOSAGE & ADMINISTRATION SECTION

Directions Initially, depress pump until primed. Hold close to mouth and spray one dose directly into mouth. Use 3 times per day. use additionally as needed.

Adult Dose 3 pump sprays

Children (2-12 years) 2 pump sprays

Reference image cough relief.jpg

Warnings

WARNINGS SECTION

If symptoms persist or worsen, or if pregnant or nursing, take only on advice of a healthcare professional. Keep out of reach of children.

Tamper resistant for your protection. Use only if safety seal is intact.

Reference image cough relief.jpg

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Reference image cough relief.jpg

Indications And Usage

INDICATIONS & USAGE SECTION

Uses for temporary relief of minor cough symptoms from the common cold or inhaled irritants:

  • Dry or hoarse cough
  • hacking, tickling or spasmodic cough
  • croupy cough and throat irritation
Reference image cough relief.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of label
Image of label

King Bio, Inc.

3 Westside Drive

Asheville, NC 28806

Questions? Call 800.543.3245

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-6166-22020-01-31C16284748780-19d75b9cf-d9b8-f424-e053-dadaa90a57ceCough Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-6166-2Cough Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-6166COUGH RELIEF (NATURAL MEDICINE) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20111129_b56c4fb1-dd6f-4425-8ac3-b9a00469cf3b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JD1
BROMINEACTIVE INGREDIENTSBV4XY874G1
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51Q1
COPPERACTIVE INGREDIENT789U1901C51
CORALLIUM RUBRUM EXOSKELETONACTIVE INGREDIENT2CA71K0DLE1
DROSERA ROTUNDIFOLIAACTIVE INGREDIENTQR44N9XPJQ1
FERROSOFERRIC PHOSPHATEACTIVE INGREDIENT91GQH8I5F71
IODINEACTIVE INGREDIENT9679TC07X41
MEPHITIS MEPHITIS ANAL GLAND FLUIDACTIVE INGREDIENT3BN57UN4US1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FM1
PROTORTONIA CACTIACTIVE INGREDIENTLZB7TFX1LT1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
RUMEX CRISPUS ROOTACTIVE INGREDIENT9N1RM2S62C1
SANGUINARIA CANADENSIS ROOTACTIVE INGREDIENTN9288CD5081
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE INGREDIENT1PIP394IID1
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139191
SULFURACTIVE INGREDIENT70FD1KFU701
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JD1
BROMINEACTIVE MOIETYSBV4XY874G1
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZB1
COPPERACTIVE MOIETY789U1901C51
CORALLIUM RUBRUM EXOSKELETONACTIVE MOIETY2CA71K0DLE1
DROSERA ROTUNDIFOLIAACTIVE MOIETYQR44N9XPJQ1
FERRIC CATIONACTIVE MOIETY91O4LML6111
IODINEACTIVE MOIETY9679TC07X41
MEPHITIS MEPHITIS ANAL GLAND FLUIDACTIVE MOIETY3BN57UN4US1
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
POTASSIUM CATIONACTIVE MOIETY295O53K1521
PROTORTONIA CACTIACTIVE MOIETYLZB7TFX1LT1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
RUMEX CRISPUS ROOTACTIVE MOIETY9N1RM2S62C1
SANGUINARIA CANADENSIS ROOTACTIVE MOIETYN9288CD5081
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE MOIETY1PIP394IID1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139191
SULFURACTIVE MOIETY70FD1KFU701
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-616657955-6166-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
7168eca7-4412-4b83-bcbf-34eefa6fef34b56c4fb1-dd6f-4425-8ac3-b9a00469cf3b2011-11-29WarningsExact identifier
spl id: 7168eca7-4412-4b83-bcbf-34eefa6fef34
spl set id: b56c4fb1-dd6f-4425-8ac3-b9a00469cf3b

Reported adverse events (FAERS/openFDA)#

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