DIO PORORO KIDS FOAMING- sodium fluoride paste, dentifrice 
Dio Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

sodium fluoride, allantoin


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


for dental care



keep out of reach of the children

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



store at room temperature


for dental use only

package label
DIO PORORO KIDS FOAMING 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75902-3001
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 g  in 100 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.05 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
XYLITOL (UNII: VCQ006KQ1E)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75902-3001-150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/04/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/04/2014
Labeler - Dio Corporation (631085206)
Registrant - Dio Corporation (631085206)
Establishment
NameAddressID/FEIBusiness Operations
KMPharmaceutical Co., Ltd.688679158manufacture(75902-3001)

Revised: 6/2017
Document Id: 50e23c08-730f-6d1a-e054-00144ff8d46c
Set id: be31c386-364e-43e6-a1d3-8ddaf8484e1c
Version: 2
Effective Time: 20170601
 
Dio Corporation