TYRAMINE- tyramine liquid 
Deseret Biologicals, Inc.

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.

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Drug Facts

ACTIVE INGREDIENTS

Tyramine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C

INDICATIONS

For temporary relief of symptoms related to tyramine sensitivity including food cravings, muscle spasm, headache, high blood pressure, excessive sweating, weight loss, fatigue, nervousness, agitation and vasodilation.

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 AND USAGE

For temporary relief of symptoms related to tyramine sensitivity including food cravings, muscle spasm, headache, high blood pressure, excessive sweating, weight loss, fatigue, nervousness, agitation and vasodilation.

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

DESBIO

NDC 43742-0201-1

HOMEOPATHIC

TYRAMINE

1 FL OZ (30 ml)

Tyramine

TYRAMINE 
tyramine liquid
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:43742-0201
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TYRAMINE (UNII: X8ZC7V0OX3) (TYRAMINE - UNII:X8ZC7V0OX3) TYRAMINE6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43742-0201-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product11/16/201212/03/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic11/16/201212/03/2019
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(43742-0201)

Revised: 3/2018
 
Deseret Biologicals, Inc.