EVERTOX SPECIAL BATH PREPARATIONS

Manufacturer
KMTR Co., Ltd.
Effective date
2015-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:20

Label at a glance#

ProductEVERTOX SPECIAL BATH PREPARATIONS
Active ingredientSILICON DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

monzonite

INACTIVE INGREDIENT SECTION

silica compound


OTC - PURPOSE SECTION

relieve atopic symptom (itching, inflammation and pain), relieve ring worm, relieve stress



OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

apply on evertox per 100 liter approximately
application part: whole body
apply for 5~30 minutes preferably during bath
keep cool and dry after use


WARNINGS SECTION

do not open the case, in case the case opened by user fault, please keep the ingredients away immediately



DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69474-1001-12020-01-31C16284748780-19d75b9cf-d5bc-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69474-1001-1EVERTOX SPECIAL BATH PREPARATIONS65 g in 1 BOTTLEPOWDER651

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69474-1001EVERTOX SPECIAL BATH PREPARATIONS (SILICON DIOXIDE) POWDER [KMTR CO., LTD.]1Legacy NDC, 1 package rows20150111_b90ce36b-2dbe-4eb5-a262-cce376ecc12f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
SILVERINACTIVE INGREDIENT3M4G523W1G1
SODIUM ALUMINIUM SILICATEINACTIVE INGREDIENT058TS43PSM1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69474-100169474-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM ALUMINIUM SILICATESODIUM ALUMINOSILICATE058TS43PSMTABLET, EXTENDED RELEASE / ORAL94 mgExact identifier — unii candidate
2 equally ranked IID candidates
SODIUM ALUMINIUM SILICATESODIUM ALUMINOSILICATE058TS43PSMTABLET / ORAL94 mgExact identifier — unii candidate
2 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
875c883b-70ab-44d2-8297-587e2e9576ddb90ce36b-2dbe-4eb5-a262-cce376ecc12f2015-01-11WarningsExact identifier
spl id: 875c883b-70ab-44d2-8297-587e2e9576dd
spl set id: b90ce36b-2dbe-4eb5-a262-cce376ecc12f

Reported adverse events (FAERS/openFDA)#

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