ACETYLCHOLINE CHLORIDE PHENOLIC- acetylcholine chloride, 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.

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Acetylcholine Chloride Phenolic

ACTIVE INGREDIENTS:  Acetylcholine Chloride 6X, 12X, 30X, 12C, 30C.

INDICATIONS:  For temporary relief of dizziness, chest congestion with mild constriction, fatigue, cough, headaches, forgetfulness and drowsiness.


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 dizziness, chest congestion with mild constriction, fatigue, cough, headaches, forgetfulness and drowsiness.


Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579

800-869-8078


PACKAGE LABEL DISPLAY:

ENERGIQUE
ACETLYCHOLINE CHLORIDE PHENOLIC
Homeopathic Remedy
1 fl. oz. (30 ml)

Acetylcholine Chloride Phenolic

ACETYLCHOLINE CHLORIDE PHENOLIC 
acetylcholine chloride, liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57520-0401
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X) ACETYLCHOLINE CHLORIDE30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57520-0401-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/07/201007/06/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic05/07/201007/06/2021
Labeler - Apotheca Company (844330915)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(57520-0401) , api manufacture(57520-0401) , label(57520-0401) , pack(57520-0401)

Revised: 6/2021
 
Apotheca Company