TRYPTOPHAN- tryptophan 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:

Tryptophan 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

INDICATIONS:

For temporary relief of symptoms related to tryptophan sensitivity including sleep disorders, bloating, colitis, poor digestion, celiac disease, flatulence, gastritis, constipation, digestive malabsorption, food sensitivities and Season Affective Disorder.

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.

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

INDICATIONS:

For temporary relief of symptoms related to tryptophan sensitivity including sleep disorders, bloating, colitis, poor digestion, celiac disease, flatulence, gastritis, constipation, digestive malabsorbtion, food sensitivities and Seasonal Affective Disorder.

QUESTIONS:

Dist. By:

Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0028-1

HOMEOPATHIC

TRYPTOPHAN

1 FL OZ (30 ml)

Tryptophan

TRYPTOPHAN
tryptophan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0028
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TRYPTOPHAN (UNII: 8DUH1N11BX) (TRYPTOPHAN - UNII:8DUH1N11BX)	TRYPTOPHAN	6 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0028-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/09/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		05/09/2012	11/10/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0028) , api manufacture(43742-0028) , label(43742-0028) , pack(43742-0028)

Revised: 6/2016

Document Id: 03ba521c-75fb-4ca3-81de-67ef0bac163b

Set id: 8952dc27-ff54-4a9c-8ed0-d7cc00fb8cda

Version: 3

Effective Time: 20160628

Deseret Biologicals, Inc.