Label: ACETYLCHOLINE CHLORIDE PHENOLIC- acetylcholine chloride, liquid
- NDC Code(s): 44911-0025-1
- Packager: Energique, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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.
Drug Label Information
Updated July 3, 2024
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- ACTIVE INGREDIENTS:
- INDICATIONS:
- WARNINGS:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- KEEP OUT OF REACH OF CHILDREN.
- INDICATIONS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY
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INGREDIENTS AND APPEARANCE
ACETYLCHOLINE CHLORIDE PHENOLIC
acetylcholine chloride, liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0025 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R) (ACETYLCHOLINE - UNII:N9YNS0M02X) ACETYLCHOLINE 6 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44911-0025-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 11/08/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/08/2012 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0025) , api manufacture(44911-0025) , label(44911-0025) , pack(44911-0025)