EXODEN CURE POWDER- aluminum chlorohydroxy allantoinate powder

Exoden Cure Powder by

Drug Labeling and Warnings

Exoden Cure Powder by is a Otc medication manufactured, distributed, or labeled by LIFEON Corp., Korea Shidenta. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Aluminum Chlorohydroxy Allantoinate 0.16%

PURPOSE

Oral Health Care

INDICATIONS & USAGE

Provide better health to teeth and gums

DOSAGE & ADMINISTRATION

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

WARNINGS

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

KEEP OUT OF REACH OF CHILDREN

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EXODEN CURE POWDER 
aluminum chlorohydroxy allantoinate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70602-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCLOXA (UNII: 18B8O9DQA2) (ALLANTOIN - UNII:344S277G0Z)	ALCLOXA	0.16 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BENTONITE (UNII: A3N5ZCN45C)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
XYLITOL (UNII: VCQ006KQ1E)
LEVOMENTHOL (UNII: BZ1R15MTK7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70602-004-02	1 in 1 CARTON	03/09/2021
1	NDC: 70602-004-01	10 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 70602-004-04	1 in 1 CARTON	03/09/2021
2	NDC: 70602-004-03	30 g in 1 CONTAINER; Type 0: Not a Combination Product
3	NDC: 70602-004-06	1 in 1 CARTON	03/09/2021
3	NDC: 70602-004-05	70 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/09/2021

Labeler - LIFEON Corp. (688528872)

Registrant - LIFEON Corp. (688528872)

Establishment
Name	Address	ID/FEI	Business Operations
Korea Shidenta		688171734	manufacture(70602-004)