NDC 58264-0035

D-35

Aconitum Napellus, Oyster Shell Calcium Carbonate, Crude, Matricaria Chamomilla, Citrullus Colocynthis Fruit Pulp, Strychnos Ignatii Seed, Delphinium Staphisagria Seed, And Bryonia Alba Root

D-35 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Aconitum Napellus; Oyster Shell Calcium Carbonate, Crude; Matricaria Chamomilla; Citrullus Colocynthis Fruit Pulp; Strychnos Ignatii Seed; Delphinium Staphisagria Seed; Bryonia Alba Root.

Product ID58264-0035_5a119e96-3ddb-4ad6-9912-80df551ac786
NDC58264-0035
Product TypeHuman Otc Drug
Proprietary NameD-35
Generic NameAconitum Napellus, Oyster Shell Calcium Carbonate, Crude, Matricaria Chamomilla, Citrullus Colocynthis Fruit Pulp, Strychnos Ignatii Seed, Delphinium Staphisagria Seed, And Bryonia Alba Root
Dosage FormSolution
Route of AdministrationSUBLINGUAL
Marketing Start Date1990-01-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameDNA Labs, Inc.
Substance NameACONITUM NAPELLUS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; MATRICARIA CHAMOMILLA; CITRULLUS COLOCYNTHIS FRUIT PULP; STRYCHNOS IGNATII SEED; DELPHINIUM STAPHISAGRIA SEED; BRYONIA ALBA ROOT
Active Ingredient Strength6 [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 58264-0035-1

29.57 mL in 1 BOTTLE, GLASS (58264-0035-1)
Marketing Start Date1990-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58264-0035-1 [58264003501]

D-35 SOLUTION
Marketing CategoryUNAPPROVED HOMEOPATHIC
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-01-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACONITUM NAPELLUS6 [hp_X]/mL

OpenFDA Data

SPL SET ID:275cc8ec-30ed-4dd9-815c-d082ee5b3a99
Manufacturer
UNII
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.