Eczema Symptom Relief

Manufacturer
King Bio Inc.
Effective date
2017-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:36

Label at a glance#

ProductEczema Symptom Relief
Active ingredientCARDIOSPERMUM HALICACABUM FLOWERING TOP, GOLDENSEAL, CENTELLA ASIATICA, ARCTIUM LAPPA ROOT, TOXICODENDRON PUBESCENS LEAF, RUMEX CRISPUS ROOT, RUTA GRAVEOLENS FLOWERING TOP, SANGUINARIA CANADENSIS ROOT, TARAXACUM OFFICINALE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts__________________________________________________________________________________________________________

HPUS active ingredient                                                                  Purpose† 

Equal volumes of each active ingredient in 10X, 20X, and 30X potencies, unless otherwise noted.

Active ingredients 50% of total weight.

Cardiospermum* (2X, 10X, 20X, 30X), Hydrastis canadensis*, Hydrastis canadensis*, Lappa major*, Rhus tox*, Rumex crispus*, Ruta graveolens*, Sanguinaria canadensis*, Taraxacum officinale*.

*Certified organic Ingredient

**"HPUS"indicates the active ingredients are in the official Homeopathic Pharmacopoeia of the United States.

INDICATIONS & USAGE SECTION

Uses for temporary relief of eczema: •redness •intense itching •allergic skin eruptions •dry or moist eruptions •thickened, crusty, scaly skin •inflamed skin •general unhealthy skin

WARNINGS SECTION

Warnings

  • For external use only. Avoid contact with eyes and broken skin.
  • Stop use and ask a doctor if •increased skin irritation or other allergic reaction develops. •symptoms worsen or do not improve within 7 days.
  • Nursing mothers should not apply to breast area.
  • Keep out of reach of children.
  • If swallowed, get medical help or contact a Poison Control Center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions

•Shake before using. •Adults & children 2 years of age and older: apply to affected area up to 4 times daily. Rub in gently. •Children under 2 years of age: consult a doctor. •Patch test recommended on sensitive skin.

OTHER SAFETY INFORMATION

Other information:

  • To open: unscrew cap, remove tube seal, replace cap.
  • Safety sealed for your protection.
  • Do not use if tube seal is missing.
  • Store at 68-77° (20-25°C).
  • Certified organic topical lotion.

INACTIVE INGREDIENT SECTION

Inactive ingredients:​ Aloe vera leaf juice powder*, avena sativa oat kernel flour*, carrageenan, chamomile​ recutita flower extract*, citrus extract*, glycerin, green tea extract*, honeysuckle extract*, lecithin*, licorice root extract*, neem seed oil*, oregon grape root extract*, organic alcohol*, oryza sativa race bran extract*, silicon dioxide, sucrose cocoate, sunflower oil*, water, xanthan gum.

*Certified organic Ingredient.

Certified organic by Oregon Tilth.

OTC - PURPOSE SECTION

__________________________________________________________________________________________________________

HPUS active ingredient                                                              Purpose†

Equal volumes of each active ingredient in 10X, 20X, and 30X potencies, unless otherwise noted.

Active ingredients 50% of total weight. 

Cardiospermum (2X, 10X, 20X, 30X)......................................................allergic skin eruption

Hydrastis canadensis..............................................................general unhealthy skin, eczema

Hydrocotyle asiatica.................................dry, eruptions, thickening of skin, exfoliation of scales

Lappa major...................................................................moist eruptions, greyish white crusts

Rhus tox........................................red, swollen, burning eczematous eruptions, scale formation

Rumex crispus.................................................................................intense itching, skin rash

Ruta graveolens......................................................................itching, inflamed, deep red skin

Sanguinaria canadensis...........................................................................redness and burning

Taraxacum officinale....................................................severe itching, skin rash, unhealthy skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-0921-32020-01-31C16284748780-19d75b9cf-ecea-f424-e053-dadaa90a57ceEczema Symptom Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-0921-3Eczema Symptom Relief1 in 1 CARTONCREAM11
57955-0921-3Eczema Symptom Relief85 g in 1 TUBECREAM851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-0921ECZEMA SYMPTOM RELIEF (CARDIOSPERMUM, HYDRASTIS CANADENSIS, HYDROCOTYLE ASIATICA, LAPPA MAJOR, RHUS TOX, RUMEX CRISPUS, RUTA GRAVEOLENS, SANGUINARIA CANADENSIS, TARAXACUM OFFICINALE) CREAM [KING BIO INC.]1Legacy NDC, 2 package rows20170301_a4751819-d243-4c0d-b381-072070c141a5.zip

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-092157955-0921-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
3e5170a1-9305-49f0-ab77-db3e2a9bbe69a4751819-d243-4c0d-b381-072070c141a52017-01-20WarningsExact identifier
spl id: 3e5170a1-9305-49f0-ab77-db3e2a9bbe69
spl set id: a4751819-d243-4c0d-b381-072070c141a5

Reported adverse events (FAERS/openFDA)#

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