Label: FRESH AQUA- ionized alkali water liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70610-107-01 - Packager: KOTUKU INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 7, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Ionized Alkali Water (99.7%)
- antibacterial
- Keep out of reach of children
- Uses Household - Every nasty smell removal occurred in household such as shoe, shelf, closet, restroom, bed, tobacco etc. - Pet odors
- Warnings Use only according to instruction When using this product Avoid direct sunlight, keep in cool place.
- Directions For hygienic disinfection, this product can be used directly to the surface.
- Inactive Ingredients Trisodium Phosphate
- FRESH AQUA
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INGREDIENTS AND APPEARANCE
FRESH AQUA
ionized alkali water liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70610-107 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 473.6 g in 475 mL Inactive Ingredients Ingredient Name Strength SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70610-107-01 475 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/13/2018 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/13/2018 Labeler - KOTUKU INC. (050192473) Registrant - KOTUKU INC. (050192473) Establishment Name Address ID/FEI Business Operations BEX INTER-CORPORATION 688504088 manufacture(70610-107)
