FRESH AQUA
- Manufacturer
- KOTUKU INC. | BEX INTER-CORPORATION
- Effective date
- 2018-08-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:56:37
Label at a glance#
ProductFRESH AQUA
Active ingredientSODIUM PHOSPHATE, TRIBASIC, DODECAHYDRATE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| efd58dcf-540a-4531-8766-e713129ca6f2 | Product name | 1 | 20250307 |
| 4b7700e3-6e0e-45e5-9d22-6f754d61386e | Product name | 2 | 20250304 |
| 726062af-1135-4707-a1d7-57256991bbf9 | Product name | 2 | 20250226 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 0ca1d589-929b-4b33-bc5b-1d84abdafa6a | Product name | 1 | 20150324 |
| fc363c46-397b-4476-ac0f-70e43e8e4592 | Product name | 1 | 20150324 |
| 19c71a3d-ed9c-166b-a7e5-38c250c35631 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70610-105-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-62b0-f424-e053-dadaa90a57ce | FRESH AQUA |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70610-105-01 | FRESH AQUA | 475 mL in 1 BOTTLE, SPRAY | LIQUID | 475 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- FRESH AQUA
- Trisodium Phosphate
- SODIUM PHOSPHATE, TRIBASIC, DODECAHYDRATE
- PHOSPHATE ION
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70610-105 | 70610-105-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM PHOSPHATE, TRIBASIC, DODECAHYDRATE | B70850QPHR | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 738089fd-716b-237e-e053-2991aa0a1a99 | 738089fd-716a-237e-e053-2991aa0a1a99 | 2018-08-14 | Warnings | 738089fd-716b-237e-e053-2991aa0a1a99 738089fd-716a-237e-e053-2991aa0a1a99 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
