PROGESTERONE PHENOLIC- progesterone, liquid
Apotheca Company

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.

----------

Progesterone Phenolic

ACTIVE INGREDIENTS: Progesterone 6X, 12X, 30X, 12C, 30C.

INDICATIONS: For temporary relief of symptoms of dairy and milk allergies, mood swings, painful menses, breast tenderness, headaches, hot flashes, and nervousness.

WARNINGS: 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.

SUGGESTED USE: 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.

INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

INDICATIONS: For temporary relief of symptoms of dairy and milk allergies, mood swings, painful menses, breast tenderness, headaches, hot flashes, and nervousness.

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579

800-869-8078

ENERGIQUE

PROGESTERONE PHENOLIC

Homeopathic Remedy

1 fl. oz. (30 ml)

Progesterone Phenolic

PROGESTERONE PHENOLIC
progesterone, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57520-0404
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y)	PROGESTERONE	30 [hp_C] 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:57520-0404-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/10/2010	09/04/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		05/10/2010	09/04/2022

Labeler - Apotheca Company (844330915)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(57520-0404) , api manufacture(57520-0404) , label(57520-0404) , pack(57520-0404)

Revised: 4/2022

Document Id: 90ef8f57-b3ba-47d1-8d5d-6e2048456bef

Set id: 69a65c2c-c361-4a54-81eb-70fcbb49fdf3

Version: 3

Effective Time: 20220406

Apotheca Company