NDC 63479-0407

D07 LMPH-DRN

Araneus Diadematus, Arisaema Triphyllum Root, Asterias Rubens, Baptisia Tinctoria, Barium Iodide, Echinacea Angustifolia, Ferrous Iodide, Goldenseal, Lachesis Muta Venom, Phytolacca Americana Root, Pinus Sylvestris Flowering Top, Scrophularia Nodosa, Spongia Officinalis Skeleton, Roasted, And Teucrium Scorodonia Flowering Top

D07 LMPH-DRN is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Apex Energetics Inc.. The primary component is Araneus Diadematus; Arisaema Triphyllum Root; Asterias Rubens; Baptisia Tinctoria Root; Barium Iodide; Echinacea Angustifolia; Ferrous Iodide; Goldenseal; Lachesis Muta Venom; Phytolacca Americana Root; Pinus Sylvestris Flowering Top; Scrophularia Nodosa; Spongia Officinalis Skeleton, Roasted; Teucrium Scorodonia Flowering Top.

Product ID63479-0407_30f580bd-aa8a-492f-9add-6b54f9956d3d
NDC63479-0407
Product TypeHuman Otc Drug
Proprietary NameD07 LMPH-DRN
Generic NameAraneus Diadematus, Arisaema Triphyllum Root, Asterias Rubens, Baptisia Tinctoria, Barium Iodide, Echinacea Angustifolia, Ferrous Iodide, Goldenseal, Lachesis Muta Venom, Phytolacca Americana Root, Pinus Sylvestris Flowering Top, Scrophularia Nodosa, Spongia Officinalis Skeleton, Roasted, And Teucrium Scorodonia Flowering Top
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1988-08-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameApex Energetics Inc.
Substance NameARANEUS DIADEMATUS; ARISAEMA TRIPHYLLUM ROOT; ASTERIAS RUBENS; BAPTISIA TINCTORIA ROOT; BARIUM IODIDE; ECHINACEA ANGUSTIFOLIA; FERROUS IODIDE; GOLDENSEAL; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS FLOWERING TOP; SCROPHULARIA NODOSA; SPONGIA OFFICINALIS SKELETON, ROASTED; TEUCRIUM SCORODONIA FLOWERING TOP
Active Ingredient Strength18 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 63479-0407-1

30 mL in 1 BOTTLE, GLASS (63479-0407-1)
Marketing Start Date1988-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63479-0407-1 [63479040701]

D07 LMPH-DRN SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1988-08-01

Drug Details


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