NDC 58264-0030

D-30

Strontium Salicylate, Methenamine, Colchicum Autumnale Bulb, Black Cohosh, Arnica Montana, Calendula Officinalis Flowering Top, Solanum Dulcamara Whole, Hypericum Perforatum, Strychnos Nux-vomica Seed, Atropa Belladonna, Echinacea Angustifolia, Hamamelis Virginiana Root Bark/stem Bark, Achillea Millefolium, And Toxicodendron Pubescens Leaf

D-30 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Strontium Salicylate; Methenamine; Colchicum Autumnale Bulb; Black Cohosh; Arnica Montana; Calendula Officinalis Flowering Top; Solanum Dulcamara Whole; Hypericum Perforatum; Strychnos Nux-vomica Seed; Atropa Belladonna; Echinacea Angustifolia; Hamamelis Virginiana Root Bark/stem Bark; Achillea Millefolium; Toxicodendron Pubescens Leaf.

Product ID58264-0030_062208eb-fcc8-4640-8876-562834d3117d
NDC58264-0030
Product TypeHuman Otc Drug
Proprietary NameD-30
Generic NameStrontium Salicylate, Methenamine, Colchicum Autumnale Bulb, Black Cohosh, Arnica Montana, Calendula Officinalis Flowering Top, Solanum Dulcamara Whole, Hypericum Perforatum, Strychnos Nux-vomica Seed, Atropa Belladonna, Echinacea Angustifolia, Hamamelis Virginiana Root Bark/stem Bark, Achillea Millefolium, And Toxicodendron Pubescens Leaf
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameSTRONTIUM SALICYLATE; METHENAMINE; COLCHICUM AUTUMNALE BULB; BLACK COHOSH; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; SOLANUM DULCAMARA WHOLE; HYPERICUM PERFORATUM; STRYCHNOS NUX-VOMICA SEED; ATROPA BELLADONNA; ECHINACEA ANGUSTIFOLIA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; ACHILLEA MILLEFOLIUM; TOXICODENDRON PUBESCENS LEAF
Active Ingredient Strength3 [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 Through2019-12-31

Packaging

NDC 58264-0030-1

29.57 mL in 1 BOTTLE, GLASS (58264-0030-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0030-1 [58264003001]

D-30 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
STRONTIUM SALICYLATE3 [hp_X]/mL

OpenFDA Data

SPL SET ID:0e74e654-4bda-4969-89be-8ab89014bce2
Manufacturer
UNII
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