PULSATILLA- pulsatilla (pratensis) 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:

(in each drop): 100% of Pulsatilla (Pratensis) 200C.

INDICATIONS:

May temporarily relieve menstrual pain, irregularity, and moodiness, especially with shifting, changeable symptoms.

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 for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

May temporarily relieve menstrual pain, irregularity, and moodiness, especially with shifting, changeable symptoms.

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

PULSATILLA

200C

1 fl. oz. (30 ml)

Pulsatilla 200C

PULSATILLA 
pulsatilla (pratensis) liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0498
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ANEMONE PRATENSIS (UNII: 8E272251DI) (ANEMONE PRATENSIS - UNII:8E272251DI) ANEMONE PRATENSIS200 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0498-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/07/2019
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0498) , api manufacture(44911-0498) , label(44911-0498) , pack(44911-0498)

Revised: 6/2019
Document Id: 2cf22f16-aaa6-4e17-81d7-48ce587dba97
Set id: 664377e7-2d2f-4a54-bfff-21ff48f7b4ee
Version: 1
Effective Time: 20190607
 
Energique, Inc.