DIO PORORO KIDS FOAMING- sodium fluoride paste, dentifrice

DIO PORORO KIDS FOAMING by

Drug Labeling and Warnings

DIO PORORO KIDS FOAMING by is a Otc medication manufactured, distributed, or labeled by Dio Corporation, KMPharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

sodium fluoride, allantoin

INACTIVE INGREDIENT

xylityl, glucosyl stevia, sodium lauroyl sarcosinate, hydroxyapatite, methylparaben, natural strawberry flavor, camellia sinensis leaf ext, water

PURPOSE

for dental care

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

spray out 1 time in mouth and gargle for 30 seconds
spray out 1 time in mouth and use toothbrush

WARNINGS

store at room temperature

DOSAGE & ADMINISTRATION

for dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIO PORORO KIDS FOAMING 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75902-3001
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.1 g  in 100 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
XYLITOL (UNII: VCQ006KQ1E)
METHYLPARABEN (UNII: A2I8C7HI9T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75902-3001-1	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/04/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/04/2014

Labeler - Dio Corporation (631085206)

Registrant - Dio Corporation (631085206)

Establishment
Name	Address	ID/FEI	Business Operations
KMPharmaceutical Co., Ltd.		688679158	manufacture(75902-3001)