Aquaflora Phase I
FDA Label NDC 57955-1601

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by King Bio Inc for the product Aquaflora Phase I (NDC 57955-1601). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding ​hpus active ingredient, ​uses, ​warnings, otc - keep out of reach of children, ​directions, ​other information, ​purpose, ​inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

​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

​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).

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