NDC 58264-0059

D-59

Fucus Vesiculosus, Spongia Officinalis Skeleton, Roasted, Graphite, Oyster Shell Calcium Carbonate, Crude, Sodium Sulfate, And Croton Oil

D-59 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Fucus Vesiculosus; Spongia Officinalis Skeleton, Roasted; Graphite; Oyster Shell Calcium Carbonate, Crude; Sodium Sulfate; Croton Oil.

Product ID58264-0059_d7ce9351-15b9-420b-b296-5d2299dea9af
NDC58264-0059
Product TypeHuman Otc Drug
Proprietary NameD-59
Generic NameFucus Vesiculosus, Spongia Officinalis Skeleton, Roasted, Graphite, Oyster Shell Calcium Carbonate, Crude, Sodium Sulfate, And Croton Oil
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameFUCUS VESICULOSUS; SPONGIA OFFICINALIS SKELETON, ROASTED; GRAPHITE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM SULFATE; CROTON OIL
Active Ingredient Strength3 [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 58264-0059-1

29.57 mL in 1 BOTTLE, GLASS (58264-0059-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0059-1 [58264005901]

D-59 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FUCUS VESICULOSUS3 [hp_X]/mL

OpenFDA Data

SPL SET ID:b153cf23-eb3b-4647-b7f4-44380d498334
Manufacturer
UNII
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.