NDC 48951-5112

Hamamelis Aesculus

Hamamelis Aesculus

Hamamelis Aesculus is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Aesculus Glabra Nut; Hamamelis Virginiana Root Bark/stem Bark; Paeonia Officinalis Root; Pulsatilla Vulgaris; Desirudin; Mercury.

Product ID48951-5112_54c6038f-1738-7417-e054-00144ff8d46c
NDC48951-5112
Product TypeHuman Otc Drug
Proprietary NameHamamelis Aesculus
Generic NameHamamelis Aesculus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc
Substance NameAESCULUS GLABRA NUT; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PAEONIA OFFICINALIS ROOT; PULSATILLA VULGARIS; DESIRUDIN; MERCURY
Active Ingredient Strength3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-5112-2

1350 PELLET in 1 BOTTLE, GLASS (48951-5112-2)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-5112-2 [48951511202]

Hamamelis Aesculus PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
AESCULUS GLABRA NUT3 [hp_X]/1

OpenFDA Data

SPL SET ID:217f677a-a5b6-4df3-97ec-0eafbc9f29ce
Manufacturer
UNII

NDC Crossover Matching brand name "Hamamelis Aesculus" or generic name "Hamamelis Aesculus"

NDCBrand NameGeneric Name
48951-5031Hamamelis AesculusHamamelis Aesculus
48951-5032Hamamelis AesculusHamamelis Aesculus
48951-5112Hamamelis AesculusHamamelis Aesculus

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.