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#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70610-107-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-6388-f424-e053-dadaa90a57ce | FRESH AQUA |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70610-107-01 | FRESH AQUA | 475 mL in 1 BOTTLE, SPRAY | LIQUID | 475 | 5 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- FRESH AQUA
- Ionized Alkali Water
- WATER
- SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70610-107 | 70610-107-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | ACTIB |
| SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS | SX01TZO3QZ | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 754e0d26-067a-cc2d-e053-2a91aa0a8541 | 754e0d26-067a-cc2d-e053-2a91aa0a8541 | 2018-09-07 | Warnings | 754e0d26-067a-cc2d-e053-2a91aa0a8541 754e0d26-067a-cc2d-e053-2a91aa0a8541 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
