INDOLE PHENOLIC- indolum liquid
Energique, 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 INGREDIENT:

Indolum 6X, 12X, 30X, 12C, 30C.

INDICATIONS:

To be used according to standard homeopathic indications.**

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

WARNINGS:

If pregnant or breastfeeding, ask a health professional before use.

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

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

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

DIRECTIONS:

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

To be used according to standard homeopathic indications.**

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

INACTIVE INGREDIENTS:

Demineralized Water, 20% Ethanol

QUESTIONS:

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579 800.868.8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

INDOLE

PHENOLIC

1 fl. oz. (30 ml)

Indole Phenolic

INDOLE PHENOLIC
indolum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:44911-0435
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:44911-0435-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/01/2017	09/05/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/01/2017	09/05/2022

Labeler - Energique, Inc. (789886132)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(44911-0435) , api manufacture(44911-0435) , label(44911-0435) , pack(44911-0435)

Revised: 6/2022

Document Id: c28d1669-88e6-43a7-a5c1-2b8b73acfcdc

Set id: f696d50d-93fe-465e-a0f0-93e36153ca73

Version: 2

Effective Time: 20220629

Energique, Inc.