AQUAFLORA PHASE II- candida albicans liquid

Aquaflora Phase II by

Drug Labeling and Warnings

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

Drug Details [pdf]

HPUS ​Active Ingredients

Candida albicans

​Uses

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

​Warnings

• ​If symptoms persist or worsen, ​seek advice of a physician.
• ​If pregnant or breast-feeding, ​ask a heathcare 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 stoach, 20 minutes before breakfast

Children(ages 2-12): One tablespoon daily under the direct supervision of a physician.

​Purpose

for temporary relief of Candida albicans

​Other Information

Tamper resistant for your protection. Use only if safety seal is intact

​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 II 
candida albicans liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57955-1602
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	6 [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: 57955-1602-6	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/03/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/03/2018

Labeler - King Bio Inc (617901350)

Registrant - King Bio Inc (617901350)

Establishment
Name	Address	ID/FEI	Business Operations
King Bio Inc		617901350	manufacture(57955-1602)