INDOLE- indolum 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.

----------

Drug Facts

ACTIVE INGREDIENTS

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

INDICATIONS

For temporary relief of bowel disorders as with colitis, celiac disease, improper digestion, and flatulence, allergies caused by pollens or foods including gluten intolerance, and/or nasal and sinus congestion, candidiasis, sleep disorders and depression.

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 AND USAGE

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

PACKAGE LABEL DISPLAY

DESBIO
NDC 43742-0212-1
HOMEOPATHIC
INDOLE
1 FL OZ (30 ml)

Indole

INDOLE
indolum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:43742-0212
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
INDOLE (UNII: 8724FJW4M5) (INDOLE - UNII:8724FJW4M5)	INDOLE	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:43742-0212-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/03/2013	08/24/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/03/2013	08/24/2020

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(43742-0212) , api manufacture(43742-0212) , label(43742-0212) , pack(43742-0212)

Revised: 9/2016

Document Id: 81a42657-5fbd-4ba1-b29b-8035c1dda385

Set id: 23e6083c-2325-43f4-b833-9ff8e33f0030

Version: 2

Effective Time: 20160928

Deseret Biologicals, Inc.