Exoden Cure Powder

Manufacturer
LIFEON Corp. | Korea Shidenta
Effective date
2022-03-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:48:40

Label at a glance#

ProductExoden Cure Powder
Active ingredientALCLOXA
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydroxy Allantoinate 0.16%

OTC - PURPOSE SECTION

Oral Health Care

INDICATIONS & USAGE SECTION

Provide better health to teeth and gums

DOSAGE & ADMINISTRATION SECTION


Wet your toothbrush, shake off surplus water and press into powder. Brush teeth thoroughly and rinse

WARNINGS SECTION

Ask a dentist before use if you have
• bleeding or redness lasting more than 2 weeks
• pain, swelling, pus, loose teeth, or more spacing between teeth
These may be signs of periodontitis, a serious form of gum disease

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT SECTION

Bentonite, Sodium Chloride, Xylitol, Chitosan, L-Menthol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70602-004-01Exoden Cure Powder10 g in 1 POUCHPOWDER102
70602-004-02Exoden Cure Powder1 in 1 CARTONPOWDER12
70602-004-03Exoden Cure Powder30 g in 1 CONTAINERPOWDER302
70602-004-04Exoden Cure Powder1 in 1 CARTONPOWDER12
70602-004-05Exoden Cure Powder70 g in 1 CONTAINERPOWDER702
70602-004-06Exoden Cure Powder1 in 1 CARTONPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70602-004EXODEN CURE POWDER (ALUMINUM CHLOROHYDROXY ALLANTOINATE) POWDER [LIFEON CORP.]2Legacy NDC, 6 package rows20220310_510c4df6-c405-4401-8bff-f5728de0fb4c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70602-00470602-004-01, 70602-004-02, 70602-004-03, 70602-004-04, 70602-004-05, 70602-004-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
d9ceb4d2-1f39-f556-e053-2a95a90a8f38510c4df6-c405-4401-8bff-f5728de0fb4c2022-03-09WarningsExact identifier
spl id: d9ceb4d2-1f39-f556-e053-2a95a90a8f38
spl set id: 510c4df6-c405-4401-8bff-f5728de0fb4c

Reported adverse events (FAERS/openFDA)#

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