L DOPA- l-dopa 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:

L-Dopa 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms such as stiff muscles, tremors, weakness, and fatigue.**

**These statements are based upon 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 a 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.

KEEP OUT OF REACH OF CHILDREN:

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

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.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms such as stiff muscles, tremors, weakness, and fatigue.**

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

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC 43742-0697-1

HOMEOPATHIC

L-DOPA

1 FL OZ (30 ml)

L-Dopa

L DOPA
l-dopa liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0697
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
LEVODOPA (UNII: 46627O600J) (LEVODOPA - UNII:46627O600J)	LEVODOPA	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:43742-0697-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	12/09/2015	06/06/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		12/09/2015	06/06/2023

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0697) , api manufacture(43742-0697) , label(43742-0697) , pack(43742-0697)

Revised: 10/2018

Document Id: e4ae37fa-9b9e-40d3-bc44-4fcfdf2ea209

Set id: dc1ed9f0-2c71-4215-a560-b6a5bd3295b2

Version: 3

Effective Time: 20181010

Deseret Biologicals, Inc.