NDC 54118-7978

Amoeba Tox

Adrenal, Amoeba Nosodes, Artemisia Absinthium

Amoeba Tox is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Abco Laboratories, Inc. The primary component is Bos Taurus Adrenal Gland; Entamoeba Histolytica; Wormwood; Adenosine Triphosphate; Baptisia Tinctoria; Cajuput Oil; Capsicum; Senna Leaf; Chelone Glabra; Cinchona Officinalis Bark; Alpine Strawberry; Gentiana Lutea Root; Goldenseal; Ceanothus Americanus Leaf; Mammal Liver; Lycopodium Clavatum Spore; Bos Taurus Mesenchyme; Strychnos Nux-vomica Seed; Quassia Amara Wood; Bos Taurus Spleen.

Product ID54118-7978_7f169fa8-7925-4baa-8fe1-644544b2a3a7
NDC54118-7978
Product TypeHuman Otc Drug
Proprietary NameAmoeba Tox
Generic NameAdrenal, Amoeba Nosodes, Artemisia Absinthium
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2012-11-28
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameABCO Laboratories, Inc
Substance NameBOS TAURUS ADRENAL GLAND; ENTAMOEBA HISTOLYTICA; WORMWOOD; ADENOSINE TRIPHOSPHATE; BAPTISIA TINCTORIA; CAJUPUT OIL; CAPSICUM; SENNA LEAF; CHELONE GLABRA; CINCHONA OFFICINALIS BARK; ALPINE STRAWBERRY; GENTIANA LUTEA ROOT; GOLDENSEAL; CEANOTHUS AMERICANUS LEAF; MAMMAL LIVER; LYCOPODIUM CLAVATUM SPORE; BOS TAURUS MESENCHYME; STRYCHNOS NUX-VOMICA SEED; QUASSIA AMARA WOOD; BOS TAURUS SPLEEN
Active Ingredient Strength6 [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_C]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_X]/60mL; [hp_Q]/60mL; [hp_X]/60mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 54118-7978-2

60 mL in 1 BOTTLE, DROPPER (54118-7978-2)
Marketing Start Date2012-11-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 54118-7978-2 [54118797802]

Amoeba Tox SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-11-28
Inactivation Date2019-11-27

Drug Details


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