THIMEROSAL
UNII 2225PI3MOV

Substance Identification & Data

This profile provides standardized clinical and technical data for Thimerosal, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 2225PI3MOV.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 54-64-8 and the RxNorm Concept ID (RxCUI) 10472. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
2225PI3MOV
CAS Registry Number
54-64-8
RxNorm Concept ID
10472

Detailed Substance Profile

Preferred Name
THIMEROSAL
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
2225PI3MOV
The specific atomic composition represented as a molecular structure string.
InChIKey
C9H9HgO2S.Na
International Chemical Identifier digital signature for unique molecular identification.
SMILES String
RTKIYNMVFMVABJ-UHFFFAOYSA-L
Line notation for describing the chemical structure and connectivity of atoms.
NCI Thesaurus
C47751
National Cancer Institute reference terminology for clinical and research data.
PubChem CID
5908
Unique identification number in the NCBI database of chemical substances.
INN ID
2548
Sequential identifier assigned via the WHO International Nonproprietary Name program.
Substance Type
chemical
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Ingredient Role
c1(C([O-])=O)c(S[Hg]CC)cccc1.[Na+]

Synonyms and Nomenclature

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

THIMEROSAL
THIOMERSAL

Common Names & Synonyms

SODIUM ETHYL(2-(MERCAPTO-.KAPPA.S)BENZOATO(2-)-.KAPPA.O)MERCURATE(1-)
SODIUM SALT OF (2-CARBOXYPHENYLTHIO)ETHYLMERCURY
THIMEROSAL [HSDB]
THIMEROSAL [II]
THIMEROSAL [JAN]
THIMEROSAL [MI]
THIMEROSAL [USP MONOGRAPH]
THIMEROSAL [USP-RS]
THIMEROSAL [VANDF]
THIOMERSAL [EP MONOGRAPH]
THIOMERSAL [INN]
THIOMERSAL [MART.]
THIOMERSAL [WHO-DD]

Brand / Trade Names

MERTHIOLATE

Systematic Nomenclature

ETHYL (SODIUM O-MERCAPTOBENZOATO)MERCURY

Technical Codes

NSC-4794

NDC Products Containing THIMEROSAL

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 5
→ Amici Pharma, Inc. 1
→ Amneal Pharmaceuticals NY LLC 1
→ Amphastar Pharmaceuticals, Inc. 1
→ Bausch & Lomb Incoporated 1
→ Bausch & Lomb Incorporated 3
→ BioActive Nutritional, Inc. 1
→ Biovem 1
→ Bryant Ranch Prepack 1
→ Central Texas Community Health Centers 1
→ DIRECT RX 1
→ Deseret Biologicals, Inc. 1
→ Endo USA, Inc. 1
→ H.J. Harkins Company, Inc. 1
→ Herbion Pakistan Pvt Ltd 1
→ Medforce Solutions Inc. 2
→ Merck Sharp & Dohme Corp. 1
→ Merck Sharp & Dohme LLC 1
→ NuCare Pharmaceuticals,Inc. 2
→ Physicians Total Care, Inc. 1
→ Preferred Pharmaceuticals Inc. 1
→ Preferred Pharmaceuticals, Inc. 2
→ Proficient Rx LP 3
→ RPK Pharmaceuticals, Inc. 3
→ Rebel Distributors Corp 5
→ Red Mountain, Inc. 1
→ RedPharm Drug 1
→ Rising Pharma Holdings, Inc. 1
→ STAT RX USA LLC 1
→ Sandoz Inc 2
→ Sandoz Inc. 1
→ SmartPractice Denmark ApS 1
→ Subsidium, LLC 1
→ Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 1

A-S Medication Solutions

NDC Product
Human Prescription Drug

Flurbiprofen Sodium
NDC 50090-3946

Generic Name
Flurbiprofen Sodium
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

Amici Pharma, Inc.

NDC Product
Human Prescription Drug

Flurbiprofen Sodium
NDC 69292-722

Generic Name
Flurbiprofen Sodium
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

Amneal Pharmaceuticals NY LLC

Amphastar Pharmaceuticals, Inc.

NDC Product
Human Prescription Drug

Amphadase
NDC 0548-9090

Generic Name
Hyaluronidase
Dosage Form
Injection
Route
Subcutaneous
Marketing
BLA
Active Listing

Bausch & Lomb Incoporated

Bausch & Lomb Incorporated

NDC Product
Human Prescription Drug

Flurbiprofen Sodium
NDC 24208-314

Generic Name
Flurbiprofen Sodium
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

BioActive Nutritional, Inc.

NDC Product
Human Otc Drug

Vax
NDC 43857-0453

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

Biovem

NDC Product

Biovem
NDC 69883-001

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

Bryant Ranch Prepack

Central Texas Community Health Centers

DIRECT RX

Deseret Biologicals, Inc.

NDC Product
Human Otc Drug

Vaxr Hc
NDC 43742-2018

Generic Name
Thuja Occidentalis, Mezereum, Silicea, Calcarea Carbonica, M...
Dosage Form
Liquid
Route
Oral
Marketing
UNAPPROVED HOMEOPATHIC
Active Listing

Endo USA, Inc.

NDC Product
Human Prescription Drug

Cortisporin Tc
NDC 63481-529

Generic Name
Colistin Sulfate, Neomycin Sulfate, Thonzonium Bromide And H...
Dosage Form
Suspension
Route
Auricular (otic)
Marketing
NDA
Active Listing

H.J. Harkins Company, Inc.

Herbion Pakistan Pvt Ltd

NDC Product

Sinosil Nasal Decongestant
NDC 44237-007

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

Medforce Solutions Inc.

NDC Product

Virx-h
NDC 69792-000

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

Virx-ra
NDC 69792-001

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

Merck Sharp & Dohme Corp.

NDC Product

Antivenin
NDC 0006-4084

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
BLA
Inactive / Discontinued

Merck Sharp & Dohme LLC

NDC Product
Plasma Derivative

Antivenin
NDC 0006-5424

Generic Name
Latrodectus Mactans
Dosage Form
Kit
Route
N/A
Marketing
BLA
Active Listing

NuCare Pharmaceuticals,Inc.

Physicians Total Care, Inc.

Preferred Pharmaceuticals Inc.

Preferred Pharmaceuticals, Inc.

Proficient Rx LP

NDC Product
Human Prescription Drug

Flurbiprofen Sodium
NDC 63187-937

Generic Name
Flurbiprofen Sodium
Dosage Form
Solution/ Drops
Route
Ophthalmic
Marketing
ANDA
Active Listing

RPK Pharmaceuticals, Inc.

Rebel Distributors Corp

NDC Product

Flurbiprofen Sodium
NDC 21695-615

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

Flurbiprofen Sodium
NDC 42254-023

Generic Name
N/A
Dosage Form
N/A
Route
N/A
Marketing
NDA AUTHORIZED GENERIC
Inactive / Discontinued

Red Mountain, Inc.

NDC Product

Bioven
NDC 69569-001

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

RedPharm Drug

Rising Pharma Holdings, Inc.

STAT RX USA LLC

Sandoz Inc

NDC Product
Human Prescription Drug

Trifluridine
NDC 61314-044

Generic Name
Trifluridine
Dosage Form
Solution
Route
Ophthalmic
Marketing
ANDA
Active Listing

Sandoz Inc.

SmartPractice Denmark ApS

Subsidium, LLC

NDC Product

Subsidium
NDC 70052-001

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

Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.

NDC Product
Human Prescription Drug

North American Coral Snake Antivenin (equine)
NDC 0008-0423

Generic Name
Coral Snake (micrurus Fulvius) Immune Globulin Antivenin (eq...
Dosage Form
Injection, Powder, For Solution
Route
Intravenous
Marketing
BLA
Active Listing

External Clinical & Regulatory Resources

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