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Aquaflora Phase I

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This product has been discontinued

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Active ingredient
Candida Albicans 30 [hp_C]/473 mL
Other brand names
Dosage form
Liquid
Route
Oral
Prescription status
Homeopathic
Marketed in the U.S.
Since 2018
Label revision date
March 20, 2018
Active ingredient
Candida Albicans 30 [hp_C]/473 mL
Other brand names
Dosage form
Liquid
Route
Oral
Prescription status
Homeopathic
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2018
Label revision date
March 20, 2018
Manufacturer
King Bio Inc
NDC root
57955-1601

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

This medication provides temporary relief from the symptoms associated with an overgrowth of Candida albicans, a type of yeast that can cause various discomforts in the body. Common symptoms of this condition may include skin reactions, a thick and cracked tongue, bad breath, dry lips and mouth, constipation, and eczema.

If you are experiencing any of these symptoms, this medication may help alleviate your discomfort. It's important to consult with a healthcare professional for proper diagnosis and treatment options tailored to your needs.

Uses

You may use this medication for the temporary relief of symptoms caused by an overgrowth of Candida albicans, a type of yeast. If you're experiencing reactions on your skin, a thick, dry, and cracked tongue, bad breath, dry lips and mouth, constipation, or eczema, this treatment could help alleviate those issues.

It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) associated with this medication. This makes it a safer option for those concerned about such risks. Always consult with your healthcare provider for personalized advice and treatment options.

Dosage and Administration

For adults aged 12 and older, you should take two tablespoons of the medication each day. It's important to do this on an empty stomach, which means you should take it 20 minutes before having breakfast. This timing helps your body absorb the medication more effectively.

If you are giving this medication to children between the ages of 2 and 12, they should take one tablespoon daily. However, it's crucial that this is done under the direct supervision of a physician (a medical doctor), ensuring that the child receives the appropriate care and monitoring.

Warnings and Precautions

If your symptoms continue or get worse, it’s important to consult with your doctor for further advice. If you are pregnant or breastfeeding, please talk to a healthcare professional before using this medication to ensure it’s safe for you and your baby.

Always prioritize your health and well-being by seeking medical guidance when needed.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's always better to be safe and get checked by a healthcare professional if you have any concerns about your health. Remember, timely intervention can make a significant difference.

Storage and Handling

To ensure your safety, always check that the safety seal on the product is intact before use. This tamper-resistant feature is designed to protect you, so do not use the product if the seal is broken or missing.

When storing the product, keep it in a cool, dry place to maintain its effectiveness. Proper handling and storage are essential for your safety and the product's performance.

Additional Information

No further information is available.

FAQ

What is the purpose of this drug?

This drug provides temporary relief of symptoms associated with Candida albicans overgrowth.

What symptoms does this drug help relieve?

It helps relieve symptoms such as skin reactions, thick and cracked tongue, bad breath, dry lips and mouth, constipation, and eczema.

What is the recommended dosage for adults?

Adults aged 12 and up should take two tablespoons daily on an empty stomach, 20 minutes before breakfast.

What is the recommended dosage for children?

Children aged 2 to 12 should take one tablespoon daily under the direct supervision of a physician.

Are there any teratogenic effects associated with this drug?

No teratogenic effects have been mentioned.

What should I do if my symptoms persist or worsen?

If your symptoms persist or worsen, seek the advice of a physician.

Is it safe to use this drug if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, consult a healthcare professional before use.

How should I check the safety of the product?

Ensure the safety seal is intact before use, as it is tamper resistant for your protection.

Packaging Info

This section summarizes the homeopathic presentations of Aquaflora Phase I (candida albicans). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aquaflora Phase I.
Details

Manufacturer Insert (PDF)

This file includes usage instructions and other product details provided by the manufacturer. This is not an FDA-approved drug.

View manufacturer document (PDF)

Description

Description:

Aquaflora Phase I is a human over-the-counter drug containing Candida albicans at a potency of 30C as the active ingredient. The formulation includes bio-energetically enhanced pure water and a blend of inactive ingredients comprising Carya ovata bark extract, citrus extract, Lonicera japonica, polylysine, and steviol glycosides. The product is administered orally and is packaged in a 473 mL plastic bottle. It is labeled under the National Drug Code (NDC) 57955-1601. The marketing of this product commenced on March 20, 2018. King Bio Inc serves as the labeler, registrant, and manufacturer, with an establishment address ID/FEI of 617901350.

Packaging & NDC

This section summarizes the homeopathic presentations of Aquaflora Phase I (candida albicans). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aquaflora Phase I.
Details

Manufacturer Insert (PDF)

This is the product document submitted by King Bio Inc for Aquaflora Phase I. It includes information on ingredients, suggested use, and labeling language. This product is not FDA-approved.

View product insert (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the manufacturer-supplied FDA Structured Product Label (DailyMed) for Aquaflora Phase I, retrieved by a validated AI data-extraction workflow.

All dosage forms and strengths provided by the manufacturer are listed in the Packaging & NDC Codes section above.

Homeopathic drug products are not reviewed by FDA for safety or effectiveness; information is reproduced without modification.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.