FRESH AQUA

Manufacturer
KOTUKU INC. | BEX INTER-CORPORATION
Effective date
2018-09-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:56:46

Label at a glance#

ProductFRESH AQUA
Active ingredientWATER
Label structure1 sections

Label contents#

Full prescribing information#

FRESH AQUA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FRESH AQUA LABEL v2FRESH AQUA LABEL v2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70610-107-012020-01-31C16284748780-19d75b9d0-6388-f424-e053-dadaa90a57ceFRESH AQUA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70610-107-01FRESH AQUA475 mL in 1 BOTTLE, SPRAYLIQUID4755

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70610-107FRESH AQUA (IONIZED ALKALI WATER) LIQUID [KOTUKU INC.]5Legacy NDC, 1 package rows20180908_754e0d26-067a-cc2d-e053-2a91aa0a8541.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70610-10770610-107-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RACTIB
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUSSX01TZO3QZIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
754e0d26-067a-cc2d-e053-2a91aa0a8541754e0d26-067a-cc2d-e053-2a91aa0a85412018-09-07WarningsExact identifier
spl id: 754e0d26-067a-cc2d-e053-2a91aa0a8541
spl set id: 754e0d26-067a-cc2d-e053-2a91aa0a8541

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.