FDA.reportPublic FDA data

Chicken Pox Symptom Relief

Manufacturer
King Bio Inc.
Effective date
2016-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:05

Label at a glance#

ProductChicken Pox Symptom Relief
Active ingredientACONITUM NAPELLUS, ANTIMONY POTASSIUM TARTRATE, APIS MELLIFERA, ATROPA BELLADONNA, CROTON TIGLIUM SEED, ECHINACEA, UNSPECIFIED, GRAPHITE, CALCIUM SULFIDE, MENTHA PIPERITA, PULSATILLA VULGARIS, RANUNCULUS BULBOSUS, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, SULFUR
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: Aconitum napellus, Antimonium tartaricum, Apis mellifica, Balladonna, Croton tiglium, Echinacea, Graphites, Hepar sulphuris calcareum, Mentha piperita, Mezereum, Pulsatilla, Ranunculus bulbosus, Rhus toxicodendron, Silicea, Sulphur. Equal volumes of each ingredient in 10X, 30X, 100X, 1M, LM1, LM2, LM3 potencies.

INDICATIONS & USAGE SECTION

Uses temporary relief of: intense itching from skin rash and vesicles (blisters), headache, fever, swollen glands, cough, sore throat, tummy ache, fatigue. Note: Intended as a complement. Not a substitute when medical care is needed.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

WARNINGS SECTION

Warnings

  • Stop use and ask your doctor if symptoms persist or worsen.
  • If pregnant or breast-feeding, ask a healthcare professional before ues.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Ages 12 and up: 3 sprays 3 times per day.
  • Children 2-12: 2 sprays 3 times per day.
  • Use additionally as needed, up to 6 times per day.

OTHER SAFETY INFORMATION

Tamper resistant for your protection. Use only if safety seal is intact. This product has not been clinically tested.

Note: Intended as a complement. Not a substitute when medical care is needed.

OTC - PURPOSE SECTION

Uses temporary relief of:

  • intense itching from skin rash and vesicles (blisters)
  • headache
  • fever
  • swollen glands
  • cough
  • sore throat
  • tummy ache
  • fatigue

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-7825-22020-01-31C16284748780-19d75b9d0-99c7-f424-e053-dadaa90a57ceChicken Pox Symptom Relief™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-7825-2Chicken Pox Symptom Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-7825CHICKEN POX SYMPTOM RELIEF (ACONITUM NAPELLUS, ANTIMONIUM TARTARICUM, APIS MELLIFICA, BALLADONNA, CROTON TIGLIUM, ECHINACEA, GRAPHITES, HEPAR SULPHURIS CALCAREUM, MENTHA PIPERITA, MEZEREUM, PULSATILLA, RANUNCULUS BULBOSUS, RHUS TOICODENDRON, SILCEA, SULPHUR) LIQUID [KING BIO INC.]1Legacy NDC, 1 package rows20160713_2748ee35-bd6c-4a2c-ae46-8120a68e0002.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-782557955-7825-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACONITUM NAPELLUSU0NQ8555JDACTIB
ANTIMONY POTASSIUM TARTRATEDL6OZ476V3ACTIB
APIS MELLIFERA7S82P3R43ZACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
CROTON TIGLIUM SEED0HK2GZK66EACTIB
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
GRAPHITE4QQN74LH4OACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
MENTHA PIPERITA79M2M2UDA9ACTIB
PULSATILLA VULGARISI76KB35JEVACTIB
RANUNCULUS BULBOSUSAEQ8NXJ0MBACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SULFUR70FD1KFU70ACTIB
WATER059QF0KO0RIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POTASSIUM SORBATE1VPU26JZZ4IACT

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
5b4243ad-bcf6-4b11-82d3-91eb25a8b8362748ee35-bd6c-4a2c-ae46-8120a68e00022016-07-13WarningsExact identifier
spl id: 5b4243ad-bcf6-4b11-82d3-91eb25a8b836
spl set id: 2748ee35-bd6c-4a2c-ae46-8120a68e0002

Reported adverse events (FAERS/openFDA)#

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