PHENYLALANINE- phenylalanine, liquid 
Apotheca Company

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.

----------

Phenylalanine

ACTIVE INGREDIENTS:  Phenylalanine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:  For temporary relief of blurred vision, mental sluggishness, mood swings, gas, headaches, chest congestion, aspartame sensitivity, hypertension, Seasonal Affective Disorder, sleep disorders, food sensitivities, depression and poor appetite.

WARNINGS:  Keep out of reach of children.  In case of overdose, contact physician or Poison Control Center right away.

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal:  "Sealed for Your Protection."  Do not use if seal is broken or missing.

DIRECTIONS:  1-10 drops under the tongue, 3 times a day or as directed by a health professional.  Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS:  For temporary relief of blurred vision, mental sluggishness, mood swings, gas headaches, chest congestion, aspartame sensitivity, hypertension, Seasonal Affective Disorder, sleep disorders, food sensitivities, depression and poor appetite.

Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com


DESBIO

NDC 57520-1039-1

HOMEOPATHIC

PHENYLALANINE

1 FL OZ (30 ml)

Phenylalanine

PHENYLALANINE 
phenylalanine, liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57520-1039
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLALANINE (UNII: 47E5O17Y3R) (PHENYLALANINE - UNII:47E5O17Y3R) PHENYLALANINE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57520-1039-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/30/201004/17/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/30/201004/17/2023
Labeler - Apotheca Company (844330915)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(57520-1039) , api manufacture(57520-1039) , label(57520-1039) , pack(57520-1039)

Revised: 3/2023
 
Apotheca Company