Progesterone Phenolic

Manufacturer: Energique, Inc. | Apotheca Company
Effective date: 2024-10-29
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:28:33

Label at a glance#

ProductProgesterone Phenolic

Active ingredientPROGESTERONE

Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Contacts and useful links#

PhoneLabel contact800-869-8078

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 24.98% of Progesterone 12X, 30X, 12C, 30C; 0.10% of Progesterone 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with reactions to progesterone, such as mood swings, painful menses, breast tenderness, headaches, hot flashes, and nervousness.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, 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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with reactions to progesterone such as mood swings, painful menses, breast tenderness, headaches, hot flashes, and nervousness.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579 800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
PROGESTERONE
PHENOLIC
1 fl. oz. (30 ml)

Progesterone Phenolic

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b46148e2-ee15-98d5-12f0-f5ec8745f6fc	Product name	3	20220927
76820076-f087-4073-b1d1-aa04b361335e	Product name	2	20220921
d3229c1a-4e51-4e04-9b13-00d24fd35242	Product name	1	20200821
213f0591-95c1-b398-40b7-08b31f66b026	Product name	4	20190206
85b2d644-53b2-f2dc-4dbc-859116ce56c0	Product name	1	20140508
d048f0e3-3c40-8816-8c5c-0ca5cd189aac	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44911-0047-1	2024-10-29	C162847	48780-1	1030e365-2d9f-111a-e063-dadaa90a10e2	DRUG FACTS:
44911-0047-1	2024-01-30	C162847	48780-1	1030e365-2d9f-111a-e063-dadaa90a10e2	DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
44911-0047-1	Progesterone Phenolic	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
44911-0047	PROGESTERONE PHENOLIC (PROGESTERONE) LIQUID [ENERGIQUE, INC.]	5	Current NDC, Legacy NDC, 1 package rows	20241031_177c7d38-d133-4e3b-a81e-f6bacd39b147.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
PROGESTERONE	ACTIVE INGREDIENT	4G7DS2Q64Y	1
PROGESTERONE	ACTIVE MOIETY	4G7DS2Q64Y	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Progesterone Phenolic
Progesterone
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
44911-0047	44911-0047-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PROGESTERONE	4G7DS2Q64Y	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii+route+dosage form 2 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Progesterone Phenolic	PROGESTERONE	Energique, Inc.	177c7d38-d133-4e3b-a81e-f6bacd39b147	2024-10-29	Warnings	Exact identifier ndc (package): 44911-0047-1 ndc (product): 44911-0047 ndc11 (package): 44911004701 spl id: 079ad30c-1a0d-475b-8043-62ad1f46fb1d spl set id: 177c7d38-d133-4e3b-a81e-f6bacd39b147

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.