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Anxiety Relief - 61727-332-21 - (ACONITUM NAPELLUS)

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Drug Information of Anxiety Relief

Product NDC: 61727-332
Proprietary Name: Anxiety Relief
Non Proprietary Name: ACONITUM NAPELLUS
Active Ingredient(s): 30; 30; 9; 9; 12; 12; 9    [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g & nbsp;   ACONITUM NAPELLUS
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Anxiety Relief

Product NDC: 61727-332
Labeler Name: Homeocare Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20111122

Package Information of Anxiety Relief

Package NDC: 61727-332-21
Package Description: 4 g in 1 TUBE (61727-332-21)

NDC Information of Anxiety Relief

NDC Code 61727-332-21
Proprietary Name Anxiety Relief
Package Description 4 g in 1 TUBE (61727-332-21)
Product NDC 61727-332
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACONITUM NAPELLUS
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 20111122
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Homeocare Laboratories
Substance Name ACONITUM NAPELLUS; ARSENIC TRIOXIDE; COFFEE BEAN; GELSEMIUM SEMPERVIRENS ROOT; MATRICARIA RECUTITA; SILVER CATION; STRYCHNOS IGNATII SEED
Strength Number 30; 30; 9; 9; 12; 12; 9
Strength Unit [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g
Pharmaceutical Classes

Complete Information of Anxiety Relief


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