Label: DIO PORORO KIDS FOAMING- sodium fluoride paste, dentifrice
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Contains inactivated NDC Code(s)
NDC Code(s): 75902-3001-1 - Packager: Dio Corporation
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated June 1, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIO PORORO KIDS FOAMING
sodium fluoride paste, dentifriceProduct 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)