NDC 70610-107

FRESH AQUA

Ionized Alkali Water

FRESH AQUA is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Kotuku Inc.. The primary component is Water.

• Product ID: 70610-107_754e0d26-067a-cc2d-e053-2a91aa0a8541
• NDC: 70610-107
• Product Type: Human Otc Drug
• Proprietary Name: FRESH AQUA
• Generic Name: Ionized Alkali Water
• Dosage Form: Liquid
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-08-13
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: KOTUKU INC.
• Substance Name: WATER
• Active Ingredient Strength: 474 g/475mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70610-107-01

475 mL in 1 BOTTLE, SPRAY (70610-107-01)

• Marketing Start Date: 2018-08-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70610-107-01 [70610010701]

FRESH AQUA LIQUID

• Marketing Category: unapproved drug other
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-13
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
WATER	473.6 g/475mL

OpenFDA Data

• SPL SET ID: 754e0d26-067a-cc2d-e053-2a91aa0a8541
• Manufacturer:
  • KOTUKU INC.
• UNII:
  • 059QF0KO0R

NDC Crossover Matching brand name "FRESH AQUA" or generic name "Ionized Alkali Water"

NDC	Brand Name	Generic Name
70610-105	FRESH AQUA	Trisodium Phosphate
70610-107	FRESH AQUA	Ionized Alkali Water
72515-100	FRESH AQUA	Trisodium Phosphate
70610-106	VEGE AQUA	Ionized Alkali Water