NDC 48951-8313

Sabadilla Eucalyptus

Sabadilla Eucalyptus

Sabadilla Eucalyptus is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Bryonia Alba Root; Eucalyptus Gum; Eupatorium Perfoliatum Flowering Top; Aconitum Napellus; Schoenocaulon Officinale Seed; Phosphorus.

Product ID48951-8313_6b172c79-6478-22cc-e053-2a91aa0afc45
NDC48951-8313
Product TypeHuman Otc Drug
Proprietary NameSabadilla Eucalyptus
Generic NameSabadilla Eucalyptus
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameBRYONIA ALBA ROOT; EUCALYPTUS GUM; EUPATORIUM PERFOLIATUM FLOWERING TOP; ACONITUM NAPELLUS; SCHOENOCAULON OFFICINALE SEED; PHOSPHORUS
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 Through2020-12-31

Packaging

NDC 48951-8313-3

60 mL in 1 BOTTLE, DROPPER (48951-8313-3)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-8313-3 [48951831303]

Sabadilla Eucalyptus LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
BRYONIA ALBA ROOT3 [hp_X]/mL

OpenFDA Data

SPL SET ID:8ee42430-817e-4fcc-8797-8842add6076e
Manufacturer
UNII

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