CUPRIC SULFATE
UNII LRX7AJ16DT

Substance Identification & Data

This profile provides standardized clinical and technical data for Cupric Sulfate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) LRX7AJ16DT.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7758-99-8 and the RxNorm Concept ID (RxCUI) 21579. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
LRX7AJ16DT
CAS Registry Number
7758-99-8
RxNorm Concept ID
21579

Detailed Substance Profile

Preferred Name
CUPRIC SULFATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
LRX7AJ16DT
The specific atomic composition represented as a molecular structure string.
InChIKey
Cu.O4S.5H2O
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
JZCCFEFSEZPSOG-UHFFFAOYSA-L
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C65354
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
24463
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
S(=O)(=O)([O-])[O-].[Cu+2].O.O.O.O.O

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Cupric Sulfate. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.

Common Names & Synonyms

COPPER (AS CUPRIC SULFATE)
COPPER (AS CUPRIC SULFATE) [VANDF]
COPPER SULFATE [EP MONOGRAPH]
COPPER SULFATE [VANDF]
COPPER SULFATE PENTAHYDRATE [EP MONOGRAPH]
COPPER SULFATE PENTAHYDRATE [WHO-DD]
COPPER(2+) SULFATE (1:1) PENTAHYDRATE
COPPER(2+) SULPHATE (1:1) PENTAHYDRATE
CUPRIC SULFATE
CUPRIC SULFATE [II]
CUPRIC SULFATE [ORANGE BOOK]
CUPRIC SULFATE [USP MONOGRAPH]
CUPRIC SULFATE [VANDF]
CUPRIC SULFATE PENTAHYDRATE
CUPRIC SULFATE PENTAHYDRATE [MI]
CUPRIC SULPHATE
CUPRIC SULPHATE PENTAHYDRATE
CUPRUM SULPHURICUM
CUPRUM SULPHURICUM [HPUS]
SULFURIC ACID COPPER(2+) SALT (1:1), PENTAHYDRATE

Systematic Nomenclature

COPPER (II) SULFATE PENTAHYDRATE
COPPER SULFATE
COPPER SULFATE PENTAHYDRATE
COPPER SULPHATE PENTAHYDRATE
COPPER(2+) SULFATE PENTAHYDRATE
COPPER(2+) SULPHATE PENTAHYDRATE
COPPER(II) SULFATE PENTAHYDRATE
COPPER(II) SULPHATE PENTAHYDRATE
SULFURIC ACID COPPER(2+) SALT (1:1), HYDRATE (1:5)

NDC Products Containing CUPRIC SULFATE

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:

Manufacturer Quick Index

→ A-S Medication Solutions 1
→ ASTONEA LABS PRIVATE LIMITED 1
→ Abeona Therapeutics Inc. 1
→ American Regent, Inc. 4
→ AmerisourceBergen Drug Corporation 1
→ Amneal Pharmaceuticals NY LLC 1
→ Asclemed USA, Inc. 1
→ Bausch & Lomb Incoporated 1
→ Blenheim Pharmacal, Inc 1
→ CarWin Pharmaceutical Associates, LLC 5
→ Carnivora Research International 1
→ Centurion Labs, LLC 1
→ Crown Laboratories 1
→ Curetech Skincare 1
→ Dabur India Limited 1
→ Deseret Biologicals, Inc. 6
→ Dolgencorp, LLC 1
→ Dr. Donna Restivo DC 1
→ Energetix Corp 1
→ Energetix Corporation 1
→ Energique, Inc. 1
→ Exeltis USA, Inc. 1
→ GRUPO TMA TECNOLOGIAS PARA EL MEJORAMIENTO DEL AGUA S.A. DE C.V. 2
→ Genuine Drugs 1
→ Guna spa 1
→ Hahnemann Laboratories, INC. 8
→ Heel Inc 5
→ J. Strickland and Co. 1
→ LJ Pharma 1
→ MediNatura Inc 2
→ Navarro Discount Pharmacies,LLC 1
→ NuCare Pharmaceuticals,Inc. 1
→ Nutrexin USA 1
→ OHM PHARMA INC. 1
→ Origin BioMed Inc. 1
→ PEKANA Naturheilmittel GmbH 1
→ Physicians Total Care, Inc. 2
→ Priyal Cosmetics 1
→ Product Quest Mfg 1
→ Proficient Rx LP 1
→ PureTek Corporation 2
→ REMEDYREPACK INC. 1
→ ROKIT HEALTHCARE Inc. 3
→ RPK Pharmaceuticals, Inc. 1
→ Rebel Distributors Corp 1
→ Rugby Laboratories 1
→ SHIELD LINE LLC 1
→ STAT Rx USA LLC 1
→ Seton Pharmaceuticals 1
→ TopCare 1
→ U.S. Pharmaceutical Corporation 2
→ US Pharmaceutical Corporation 1
→ United Exchange Corp. 1
→ Uriel Pharmacy Inc. 9
→ Uriel Pharmacy, Inc. 3
→ VIATREXX BIO INCORPORATED 1
→ Veridian Healthcare 3
→ Walgreens Company 1

A-S Medication Solutions

ASTONEA LABS PRIVATE LIMITED

Abeona Therapeutics Inc.

NDC Product
Human Prescription Drug

Zevaskyn
NDC 84103-007

Generic Name
Prademagene Zamikeracel
Dosage Form
Cellular Sheet
Route
Topical
Marketing
BLA
Active Listing

American Regent, Inc.

NDC Product
Human Prescription Drug

Multitrace-5
NDC 0517-8510

Generic Name
Trace Elements 5
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multitrace -4 Pediatric
NDC 0517-9203

Generic Name
Trace Elements 4
Dosage Form
Injection, Solution, Concentrate
Route
Intravenous
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multrys
NDC 0517-9302

Generic Name
Trace Elements Injection 4
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing
NDC Product
Human Prescription Drug

Tralement
NDC 0517-9305

Generic Name
Trace Elements Injection 4
Dosage Form
Injection, Solution
Route
Intravenous
Marketing
NDA
Active Listing

AmerisourceBergen Drug Corporation

Amneal Pharmaceuticals NY LLC

Asclemed USA, Inc.

Bausch & Lomb Incoporated

Blenheim Pharmacal, Inc

CarWin Pharmaceutical Associates, LLC

NDC Product

Quflora Pediatric Drops
NDC 15370-100

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product

Quflora Pediatric Drops
NDC 15370-101

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued
NDC Product
Human Prescription Drug

Quflora Pediatric
NDC 15370-103

Generic Name
Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-t...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Quflora Pediatric
NDC 15370-104

Generic Name
Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-t...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Quflora Pediatric
NDC 15370-105

Generic Name
Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-t...
Dosage Form
Tablet, Chewable
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

Carnivora Research International

NDC Product
Human Otc Drug

Lymph Drainage
NDC 69134-0002

Generic Name
Baptisia Tinctoria, Citrus Limonum, Echinacea (angustifolia)...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Centurion Labs, LLC

NDC Product

C-nate Dha
NDC 23359-105

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

Crown Laboratories

NDC Product
Human Otc Drug

Mineral Ice Pain Relieving
NDC 0316-0226

Generic Name
Menthol
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Curetech Skincare

Dabur India Limited

NDC Product
Human Otc Drug

Cold Ice Analgesic Gel
NDC 68747-3021

Generic Name
Menthol
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

Deseret Biologicals, Inc.

NDC Product
Human Otc Drug

Detox Ii
NDC 43742-1490

Generic Name
Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, E...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product
Human Otc Drug

Energy Catalyst
NDC 43742-1948

Generic Name
Viscum Album, Cobalt Gluconate, Cuprum Sulphuricum, Ferrous ...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product
Human Otc Drug

Bio Placenta Phase
NDC 43742-1954

Generic Name
Aesculus Hippocastanum, Sarcolacticum Acidum, Cuprum Sulphur...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product
Human Otc Drug

Detox Ii
NDC 43742-2038

Generic Name
Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, E...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Energy Catalyst
NDC 43742-2203

Generic Name
Adenosinum Cyclophosphoricum, Alumina, Arsenicum Album, Ceri...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Bio Placenta Phase
NDC 43742-2240

Generic Name
Aesculus Hippocastanum, Arteria Suis, Astragalus Exscapus, B...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Dolgencorp, LLC

NDC Product

Rexall Ice Cold Analgesic
NDC 55910-088

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

Dr. Donna Restivo DC

NDC Product
Human Otc Drug

D2 Organ Support
NDC 62185-0061

Generic Name
Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, E...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Energetix Corp

NDC Product

Agri-chord
NDC 64578-0055

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

Energetix Corporation

NDC Product
Human Otc Drug

Agri-chord
NDC 64578-0156

Generic Name
Arsenicum Alb, Belladonna, Calc Carb, Ceanothus, Chelidonium...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Energique, Inc.

NDC Product
Human Otc Drug

Trace Mineral Cord
NDC 44911-0724

Generic Name
Argentum Metallicum, Aurum Metallicum, Boron Citrate, Calcar...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Exeltis USA, Inc.

NDC Product
Human Prescription Drug

Strovite One Caplets
NDC 0642-0207

Generic Name
Vitamin A, Calcium Pantothenate, Ascorbic Acid, Cholecalcife...
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

GRUPO TMA TECNOLOGIAS PARA EL MEJORAMIENTO DEL AGUA S.A. DE C.V.

NDC Product

Aquatec Alonglife
NDC 80224-1000

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
NDC Product

Nano - Q1
NDC 80224-2000

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

Genuine Drugs

NDC Product

Blue Ice Pain Relieving
NDC 69666-368

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

Guna spa

NDC Product
Human Otc Drug

Guna-cell
NDC 17089-450

Generic Name
Acetylcarnitine, L-ampc-alpha-lipoic Ac-a-tocopherol-ascorbi...
Dosage Form
Solution/ Drops
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Hahnemann Laboratories, INC.

NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2894

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2895

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2896

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2897

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2898

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2899

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2900

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 37662-2901

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Heel Inc

NDC Product

Solidago Compositum
NDC 50114-0110

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Spascupreel
NDC 50114-6129

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Placenta Compositum
NDC 50114-7055

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Nectadyn
NDC 50114-8510

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Reboost
NDC 50114-8550

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

J. Strickland and Co.

LJ Pharma

NDC Product
Human Otc Drug

Wish Ultra Winter Ice
NDC 84809-008

Generic Name
Menthol
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

MediNatura Inc

NDC Product
Human Otc Drug

Bhi Spasm Pain
NDC 62795-1015

Generic Name
Atropine Sulfate, Aconitum Napellus, Bryonia Alba Root, Citr...
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing
NDC Product

Spascupreel
NDC 62795-9493

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

Navarro Discount Pharmacies,LLC

NDC Product

Blue Ice Pain Relieving
NDC 59970-073

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

NuCare Pharmaceuticals,Inc.

Nutrexin USA

NDC Product

Iron Therapy
NDC 69173-0001

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

OHM PHARMA INC.

NDC Product
Human Otc Drug

Cuprum Sulphuricum
NDC 66096-827

Generic Name
Cuprum Sulphuricum
Dosage Form
Pellet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Origin BioMed Inc.

NDC Product

Bionica Pain Relieving Gel
NDC 15377-012

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

PEKANA Naturheilmittel GmbH

NDC Product
Human Otc Drug

Ferrodonna
NDC 59469-122

Generic Name
Arsenic Trioxide, Ceanothus Americanus Leaf, Cinchona Offici...
Dosage Form
Solution/ Drops
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Physicians Total Care, Inc.

Priyal Cosmetics

Product Quest Mfg

NDC Product

Therapeutic Menthol
NDC 64048-5117

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

Proficient Rx LP

PureTek Corporation

NDC Product
Human Prescription Drug

Purevit Dualfe Plus
NDC 59088-112

Generic Name
Ferrous Fumarate, Polysaccharide Iron Complex
Dosage Form
Capsule
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Dexatran
NDC 59088-643

Generic Name
Multivitamin
Dosage Form
Capsule
Route
Cutaneous; Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

REMEDYREPACK INC.

ROKIT HEALTHCARE Inc.

NDC Product

Aqua De Folli Hair Booster
NDC 80592-202

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

RPK Pharmaceuticals, Inc.

Rebel Distributors Corp

Rugby Laboratories

NDC Product
Human Otc Drug

Rugby Ice Blue External Analgesic
NDC 0536-1061

Generic Name
Menthol, Unspecified Form
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

SHIELD LINE LLC

NDC Product
Human Otc Drug

Medpride Cold Ice Analgesic Gel
NDC 52410-3021

Generic Name
Menthol
Dosage Form
Gel
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

STAT Rx USA LLC

Seton Pharmaceuticals

NDC Product
Human Prescription Drug

Se-tan Plus
NDC 13925-118

Generic Name
Multivitamin/mineral
Dosage Form
Capsule, Gelatin Coated
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

TopCare

NDC Product

Therapeutic Ice
NDC 36800-879

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

U.S. Pharmaceutical Corporation

NDC Product
Human Prescription Drug

Concept Ob
NDC 52747-620

Generic Name
Vitamin Mineral Supplement
Dosage Form
Capsule
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Concept Dha
NDC 52747-621

Generic Name
Vitamin- Mineral Omega-3 Supplement
Dosage Form
Capsule, Liquid Filled
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

US Pharmaceutical Corporation

NDC Product

Tandem Plus
NDC 52747-902

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED DRUG OTHER
Inactive / Discontinued

United Exchange Corp.

NDC Product

Coralite Blue Ice
NDC 65923-157

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH NOT FINAL
Inactive / Discontinued

Uriel Pharmacy Inc.

NDC Product

Cuprum Sulfuricum 6
NDC 48951-3146

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Eucalyptus Cuprum Sulf.
NDC 48951-4046

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Phosphorus Comp.
NDC 48951-8029

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Phosphorus Comp.
NDC 48951-8030

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Thyreoidea Melissa
NDC 48951-9014

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Veratrum Chamomilla
NDC 48951-9037

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Veratrum Chamomilla
NDC 48951-9038

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Thyreoidea Belladonna
NDC 48951-9357

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

Uriel Pharmacy, Inc.

NDC Product

Argentum Veratrum
NDC 48951-1358

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Borago Lavender Cum Cupro
NDC 48951-2153

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued
NDC Product

Thyreoidea Belladonna
NDC 48951-9356

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

VIATREXX BIO INCORPORATED

NDC Product

Intra-cell
NDC 63776-250

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
UNAPPROVED HOMEOPATHIC
Inactive / Discontinued

Veridian Healthcare

Walgreens Company

NDC Product

Walgreens Ice Blue Gel
NDC 0363-9621

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
OTC MONOGRAPH DRUG
Inactive / Discontinued

External Clinical & Regulatory Resources

CAS
Common Chemistry
NCATS
Inxight Drugs
NLM
DailyMed Products
NCATS
GSRS Full Record
NIH
NCI Thesaurus
NLM
PubChem Compound