MANGANESE SULFATE
UNII W00LYS4T26

Substance Identification & Data

This profile provides standardized clinical and technical data for Manganese Sulfate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) W00LYS4T26.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 10034-96-5 and the RxNorm Concept ID (RxCUI) 29268. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
W00LYS4T26
CAS Registry Number
10034-96-5
RxNorm Concept ID
29268

Detailed Substance Profile

Preferred Name
MANGANESE SULFATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
W00LYS4T26
The specific atomic composition represented as a molecular structure string.
InChIKey
Mn.O4S.H2O
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
ISPYRSDWRDQNSW-UHFFFAOYSA-L
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C66054
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
177577
Unique identification number in the NCBI database of chemical substances.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
[Mn+2].O=S(=O)([O-])[O-].O

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Manganese 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.

FDA Official Name

MANGANESE SULFATE

Common Names & Synonyms

MANGANESE SULFATE [FCC]
MANGANESE SULFATE [MART.]
MANGANESE SULFATE [ORANGE BOOK]
MANGANESE SULFATE [USP IMPURITY]
MANGANESE SULFATE [USP MONOGRAPH]
MANGANESE SULFATE [VANDF]
MANGANESE SULFATE MONOHYDRATE [EP MONOGRAPH]
MANGANESE SULFATE MONOHYDRATE [MI]
MANGANESE SULFATE MONOHYDRATE [WHO-DD]
MANGANESE(2+) SULFATE (1:1) MONOHYDRATE
MANGANESE(2+) SULPHATE (1:1) MONOHYDRATE
MANGANUM SULPHURICUM
MANGANUM SULPHURICUM [HPUS]
SULFURIC ACID, MANGANESE(2+) SALT (1:1) MONOHYDRATE

Systematic Nomenclature

MANGANESE SULFATE MONOHYDRATE
MANGANESE SULPHATE
MANGANESE SULPHATE MONOHYDRATE

NDC Products Containing MANGANESE SULFATE

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

Manufacturer Quick Index

→ AMOREPACIFIC CORPORATION 1
→ Abeona Therapeutics Inc. 1
→ American Regent, Inc. 3
→ Amorepacific Corporation 1
→ Attuned Matrix, LLC 1
→ BM Private Limited 1
→ Bestmade Natural Products 1
→ Blue Heron Pharmaceuticals, LLC 1
→ COSVISION 1
→ Casmara Cosmetics, SA 2
→ Centurion Labs, LLC 1
→ Dr. Masood Homeopathic Pharmaceuticals Private Limited 1
→ Hahnemann Laboratories, INC. 7
→ Novian Pharmaceuticals 1
→ PureTek Corporation 23
→ Seton Pharmaceuticals 1
→ Sun Bum LLC 1
→ Sun Bum, LLC 1
→ U.S. Pharmaceutical Corporation 1
→ US Pharmaceutical Corporation 1

AMOREPACIFIC CORPORATION

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

Amorepacific Corporation

NDC Product

Laneige Hydro Uv Defense
NDC 43419-768

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

Attuned Matrix, LLC

NDC Product
Human Otc Drug

Mens Sports Formula
NDC 71144-0002

Generic Name
Agnus Castus, Arnica Montana, Arsenicum Album, Aurum Muriati...
Dosage Form
Spray
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

BM Private Limited

NDC Product
Human Otc Drug

Bm Manganese Sulfate (mang Sulf)
NDC 85816-1035

Generic Name
Manganese Sulfate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Bestmade Natural Products

Blue Heron Pharmaceuticals, LLC

NDC Product
Human Prescription Drug

Matronex
NDC 85622-200

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing

COSVISION

Casmara Cosmetics, SA

Centurion Labs, LLC

NDC Product

Centratex
NDC 23359-100

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

Dr. Masood Homeopathic Pharmaceuticals Private Limited

NDC Product

Enerjizer
NDC 82797-423

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

Hahnemann Laboratories, INC.

NDC Product
Human Otc Drug

Manganum Sulphuricum
NDC 37662-1553

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

Manganum Sulphuricum
NDC 37662-1554

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

Manganum Sulphuricum
NDC 37662-1555

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

Manganum Sulphuricum
NDC 37662-1556

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

Manganum Sulphuricum
NDC 37662-1557

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

Manganum Sulphuricum
NDC 37662-1558

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

Manganum Sulphuricum
NDC 37662-1559

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

Novian Pharmaceuticals

NDC Product

Keylosa
NDC 83146-003

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

PureTek Corporation

NDC Product
Human Prescription Drug

Multitol-m
NDC 59088-005

Generic Name
Multivitamin, Folate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Finazol
NDC 59088-008

Generic Name
Ferrous Fumarate, Folate
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prenatol-m
NDC 59088-009

Generic Name
Multivitamin
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
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

Vitrexyl
NDC 59088-164

Generic Name
Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitrexyl Plus Iron
NDC 59088-165

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prenatrix
NDC 59088-166

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitrexate
NDC 59088-167

Generic Name
Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitrexate Fe
NDC 59088-168

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Prenatryl
NDC 59088-169

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitranol Fe
NDC 59088-173

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Venexa
NDC 59088-176

Generic Name
Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Venexa Fe
NDC 59088-177

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Pretrate
NDC 59088-178

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Zintrexyl-c
NDC 59088-180

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Folitin-z
NDC 59088-181

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ribotin-e
NDC 59088-182

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ventrixyl
NDC 59088-186

Generic Name
Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Ventrixyl Fe
NDC 59088-187

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Vitramyn
NDC 59088-193

Generic Name
Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Foliflex
NDC 59088-480

Generic Name
Ferrous Fumarate, Folic Acid
Dosage Form
Tablet
Route
Oral
Marketing
UNAPPROVED DRUG OTHER
Active Listing
NDC Product
Human Prescription Drug

Multitam
NDC 59088-525

Generic Name
Folic Acid
Dosage Form
Tablet
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

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

Sun Bum LLC

Sun Bum, LLC

NDC Product
Human Otc Drug

Sun Bum 15 Premium Sunscreen Browning
NDC 69039-801

Generic Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage Form
Lotion
Route
Topical
Marketing
OTC MONOGRAPH DRUG
Active Listing

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

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

External Clinical & Regulatory Resources

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