Indications and uses
for temporary relief of Candida albicans overgrowt symptoms, such as: reactions on skin thick, dry, and cracked tongue bad breath dry lips and mouth constipation eczema
Aquaflora Phase I
- Manufacturer
- King Bio Inc
- Effective date
- 2018-03-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:09:17
Label at a glance#
ProductAquaflora Phase I
Active ingredientCANDIDA ALBICANS
Label structure9 sections
Dosage and administration
Adults (12 & up): Two tablespoons daily on an empty stomach, 20 minutes before breakfast. Children(ages 2-12): One tablespoon daily under the direct supervision of a physician.
Label contents#
Full prescribing information#
HPUS Active Ingredient
Candida albicans 30C
Uses
for temporary relief of Candida albicans overgrowt symptoms, such as:
- reactions on skin
- thick, dry, and cracked tongue
- bad breath
- dry lips and mouth
- constipation
- eczema
Warnings
If symptoms persist or worsen, seek advice of a physician
If pregnant or breast-feeding, ask a healthcare professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children
Directions
Adults (12 & up): Two tablespoons daily on an empty stomach, 20 minutes before breakfast.
Children(ages 2-12): One tablespoon daily under the direct supervision of a physician.
Other Information
Tamper resistant for your protection. Use only if safety seal is intact.
Purpose
for temporary relief of Candida albicans overgrowth symptoms, such as: reactions on skin, thick, dry and cracked tongue, bad breath, dry lips and mouth, constipation, eczema
Inactive Ingredients
Bio-Energetically Enhanced pure water, Carya ovata bark extract (hickory), citrus extract, Lonicera japonica (honeysuckle), polylysine (natural ferment), steviol glycosides (stevia).
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57955-1601-6 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-1968-f424-e053-dadaa90a57ce | Aquaflora Phase I |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57955-1601-6 | Aquaflora Phase I | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 57955-1601 | AQUAFLORA PHASE I (CANDIDA ALBICANS) LIQUID [KING BIO INC] | 1 | Legacy NDC, 1 package rows | 20180320_2e36efd7-0905-490d-9400-6d988a59c7d3.zip |
Products#
Every source-derived product name is available through these pages.
- Aquaflora Phase I
- Candida albicans
- WATER
- CARYA OVATA BARK
- CITRUS BIOFLAVONOIDS
- LONICERA JAPONICA FLOWER
- POLYEPSILON-LYSINE (4000 MW)
- REBAUDIOSIDE A
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 57955-1601 | 57955-1601-6 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CANDIDA ALBICANS | 4D7G21HDBC | ACTIB |
| WATER | 059QF0KO0R | IACT |
| CARYA OVATA BARK | X765CF609L | IACT |
| CITRUS BIOFLAVONOIDS | BD70459I50 | IACT |
| LONICERA JAPONICA FLOWER | 4465L2WS4Y | IACT |
| POLYEPSILON-LYSINE (4000 MW) | WB0M8X4TWR | IACT |
| REBAUDIOSIDE A | B3FUD0528F | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.