PULSATILLA 30C- pulsatilla (vulgaris) 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) Pulsatilla 30C 100%

PURPOSE

Pulsatilla 30C - moodiness**

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

USES:

May temporarily relieve: • menstrual pain • irregularity • moodiness • especially with shifting, changeable symptoms**** Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

Stop use and ask a doctor if symptoms persist for more than 7 days.

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:

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. • Consult a physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol

QUESTIONS:

Dist. by Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579

800.869.8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

PULSATILLA

30C

1 fl. oz. (30 ml)

PULSATILLA  30C
PULSATILLA  30C
pulsatilla (vulgaris) liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0696
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) PULSATILLA VULGARIS WHOLE30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0696-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/04/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/04/2024
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0696) , api manufacture(44911-0696) , label(44911-0696) , pack(44911-0696)

Revised: 1/2024
Document Id: 7990817b-5880-4132-ac43-f45e5031cff2
Set id: 0cd5927c-16cb-4a7a-8849-32156479fe77
Version: 1
Effective Time: 20240104
 
Energique, Inc.