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
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELATONIN (UNII: JL5DK93RCL) (MELATONIN - UNII:JL5DK93RCL) MELATONIN 6 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0205-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 12/17/2012
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 12/17/2012 04/21/2021
Labeler - Deseret Biologicals, Inc. (940741853)
Registrant - Apotheca Company (844330915)
Establishment
Name Address ID/FEI Business Operations
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.