MELATONIN- melatonin 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

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

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to sleep disorders, Seasonal Affective Disorder, jet lag, and depression.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS

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

If pregnant or breast-feeding, ask 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.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms related to sleep disorders, Seasonal Affective Disorder, jet lag, and depression.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0205-1

HOMEOPATHIC

MELATONIN

1 FL OZ (30 ml)

Melatonin

MELATONIN
melatonin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0205
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MELATONIN (UNII: JL5DK93RCL) (MELATONIN - UNII:JL5DK93RCL)	MELATONIN	6 [hp_X] in 1 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:43742-0205-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	12/17/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		12/17/2012	04/21/2021

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0205) , api manufacture(43742-0205) , label(43742-0205) , pack(43742-0205)

Revised: 6/2016

Document Id: a02d2040-67c7-40d6-8725-f774db2408c4

Set id: bb074765-ca7c-4c30-bd6f-b2292f0abb96

Version: 3

Effective Time: 20160628

Deseret Biologicals, Inc.