AQUAFLORA PHASE I- candida albicans liquid

Aquaflora Phase I by

Drug Labeling and Warnings

Aquaflora Phase I by is a Homeopathic medication manufactured, distributed, or labeled by King Bio Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

​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.

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).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AQUAFLORA PHASE I 
candida albicans liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57955-1601
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	30 [hp_C]  in 473 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARYA OVATA BARK (UNII: X765CF609L)
CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
POLYEPSILON-LYSINE (4000 MW) (UNII: WB0M8X4TWR)
REBAUDIOSIDE A (UNII: B3FUD0528F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57955-1601-6	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/20/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/20/2018

Labeler - King Bio Inc (617901350)

Registrant - King Bio Inc (617901350)

Establishment
Name	Address	ID/FEI	Business Operations
King Bio Inc		617901350	manufacture(57955-1601)