NDC 58264-0008

D-8

Spongia Officinalis Skeleton, Roasted, Causticum, Lachesis Muta Venom, Calcium Sulfide, Thymus Serpyllum, Antimony Potassium Tartrate, Aconitum Napellus, And Drosera Rotundifolia

D-8 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Spongia Officinalis Skeleton, Roasted; Causticum; Lachesis Muta Venom; Calcium Sulfide; Thymus Serpyllum; Antimony Potassium Tartrate; Aconitum Napellus; Drosera Rotundifolia.

Product ID58264-0008_4ca9c110-4eda-4dc9-a873-f154625833b4
NDC58264-0008
Product TypeHuman Otc Drug
Proprietary NameD-8
Generic NameSpongia Officinalis Skeleton, Roasted, Causticum, Lachesis Muta Venom, Calcium Sulfide, Thymus Serpyllum, Antimony Potassium Tartrate, Aconitum Napellus, And Drosera Rotundifolia
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameSPONGIA OFFICINALIS SKELETON, ROASTED; CAUSTICUM; LACHESIS MUTA VENOM; CALCIUM SULFIDE; THYMUS SERPYLLUM; ANTIMONY POTASSIUM TARTRATE; ACONITUM NAPELLUS; DROSERA ROTUNDIFOLIA
Active Ingredient Strength4 [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 Through2019-12-31

Packaging

NDC 58264-0008-1

29.57 mL in 1 BOTTLE, GLASS (58264-0008-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0008-1 [58264000801]

D-8 SOLUTION
Marketing CategoryUnapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SPONGIA OFFICINALIS SKELETON, ROASTED4 [hp_X]/mL

OpenFDA Data

SPL SET ID:bc817ccf-f11c-4875-9e14-5a249f92c503
Manufacturer
UNII
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.