Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, USP Sterile

Manufacturer
Somerset Therapeutics, LLC | Somerset Therapeutics Private Limited
Effective date
2024-08-06
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 21:09:43

Label at a glance#

Productpolymyxin b sulfate and trimethoprim sulfate
Active ingredientPOLYMYXIN B SULFATE, TRIMETHOPRIM
Label structure10 sections

Indications and uses

Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, USP is indicated in the treatment of surface ocular bacterial infections, including acute bacterial conjunctivitis, and blepharoconjunctivitis, caused by susceptible strains of the following microorganisms: Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Streptococcus viridans, Haemophilus influenzae and Pseudomonas aeruginosa. ...

Dosage and administration

In mild to moderate infections, instill one drop in the affected eye(s) every three hours (maximum of 6 doses per day) for a period of 7 to 10 days.

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, USP is a sterile antimicrobial solution for topical ophthalmic use. It has pH of 4.0 to 6.2 and osmolality of 270 to 310 mOsm/kg.

Chemical Names:

Trimethoprim, 5-(3,4,5-Trimethoxybenzyl)pyrimidine-2,4-,diamine, is a white, odorless, crystalline powder with a molecular weight of 290.3 and the following structural formula:

Structure
Structure

Polymyxin B sulfate is the sulfate salt of polymyxin B1 and B2 which are produced by the growth of Bacillus polymyxa (Prazmowski) Migula (Fam. Bacillaceae). It has a potency of not less than 6,000 polymyxin B units per mg, calculated on an anhydrous basis. The structural formulae are:

Structure
Structure

Contains: Actives: polymyxin B sulfate 10,000 units/mL; trimethoprim sulfate equivalent to trimethoprim 1 mg/mL. Preservative: benzalkonium chloride 0.04 mg/mL. Inactives: water for injection; sodium chloride; and sulfuric acid. May also contain sodium hydroxide to adjust the pH.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Trimethoprim is a synthetic antibacterial drug active against a wide variety of aerobic gram-positive and gram-negative ophthalmic pathogens. Trimethoprim blocks the production of tetrahydrofolic acid from dihydrofolic acid by binding to and reversibly inhibiting the enzyme dihydrofolate reductase. This binding is stronger for the bacterial enzyme than for the corresponding mammalian enzyme and therefore selectively interferes with bacterial biosynthesis of nucleic acids and proteins.

Polymyxin B, a cyclic lipopeptide antibiotic, is bactericidal for a variety of gram-negative organisms, especially Pseudomonas aeruginosa. It increases the permeability of the bacterial cell membrane by interacting with the phospholipid components of the membrane.

Blood samples were obtained from 11 human volunteers at 20 minutes, 1 hour and 3 hours following instillation in the eye of 2 drops of ophthalmic solution containing 1 mg trimethoprim and 10,000 units polymyxin B per mL. Peak serum concentrations were approximately 0.03 mcg/mL trimethoprim and 1 unit/mL polymyxin B.

Microbiology: In vitro studies have demonstrated that the anti-infective components of polymyxin B sulfate and trimethoprim are active against the following bacterial pathogens that are capable of causing external infections of the eye:

Trimethoprim: Staphylococcus aureus and Staphylococcus epidermidis, Streptococcus pyogenes, Streptococcus faecalis, Streptococcus pneumoniae, Haemophilus influenzae, Haemophilus aegyptius, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis (indole-negative), Proteus vulgaris (indole-positive), Enterobacter aerogenes and Serratia marcescens.

Polymyxin B: Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Enterobacter aerogenes and Haemophilus influenzae.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, USP is indicated in the treatment of surface ocular bacterial infections, including acute bacterial conjunctivitis, and blepharoconjunctivitis, caused by susceptible strains of the following microorganisms: Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus pneumoniae, Streptococcus viridans, Haemophilus influenzae and Pseudomonas aeruginosa. *

*Efficacy for this organism in this organ system was studied in fewer than 10 infections.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution is contraindicated in patients with known hypersensitivity to any of its components.

WARNINGS

WARNINGS SECTION

NOT FOR INJECTION INTO THE EYE. If a sensitivity reaction to polymyxin B sulfate and trimethoprim ophthalmic solution occurs, discontinue use. Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution is not indicated for the prophylaxis or treatment of ophthalmia neonatorum.

PRECAUTIONS

PRECAUTIONS SECTION

General:

As with other antimicrobial preparations, prolonged use may result in overgrowth of nonsusceptible organisms, including fungi. If superinfection occurs, appropriate therapy should be initiated.

Information for Patients:

INFORMATION FOR PATIENTS SECTION

Avoid contaminating the applicator tip with material from the eye, fingers, or other source. This precaution is necessary if the sterility of the drops is to be maintained.

If redness, irritation, swelling or pain persists or increases, discontinue use immediately and contact your physician. Patients should be advised not to wear contact lenses if they have signs and symptoms of ocular bacterial infections.

Carcinogenesis, Mutagenesis, Impairment of Fertility:

Carcinogenesis: Long-term studies in animals to evaluate carcinogenic potential have not been conducted with polymyxin B sulfate or trimethoprim.

Mutagenesis: Trimethoprim was demonstrated to be non-mutagenic in the Ames assay. In studies at two laboratories no chromosomal damage was detected in cultured Chinese hamster ovary cells at concentrations approximately 500 times human plasma levels after oral administration; at concentrations approximately 1,000 times human plasma levels after oral administration in these same cells, a low level of chromosomal damage was induced at one of the laboratories. Studies to evaluate mutagenic potential have not been conducted with polymyxin B sulfate.

Impairment of Fertility: Polymyxin B sulfate has been reported to impair the motility of equine sperm, but its effects on male or female fertility are unknown.

No adverse effects on fertility or general reproductive performance were observed in rats given trimethoprim in oral dosages as high as 70 mg/kg/day for males and 14 mg/kg/day for females.

Pregnancy:

PREGNANCY SECTION

Teratogenic Effects: Animal reproduction studies have not been conducted with polymyxin B sulfate. It is not known whether polymyxin B sulfate can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.

Trimethoprim has been shown to be teratogenic in the rat when given in oral doses 40 times the human dose. In some rabbit studies, the overall increase in fetal loss (dead and resorbed and malformed conceptuses) was associated with oral doses 6 times the human therapeutic dose.

While there are no large well-controlled studies on the use of trimethoprim in pregnant women, Brumfitt and Pursell, in a retrospective study, reported the outcome of 186 pregnancies during which the mother received either placebo or oral trimethoprim in combination with sulfamethoxazole. The incidence of congenital abnormalities was 4.5% (3 of 66) in those who received placebo and 3.3% (4 of 120) in those receiving trimethoprim and sulfamethoxazole. There were no abnormalities in the 10 children whose mothers received the drug during the first trimester. In a separate survey, Brumfitt and Pursell also found no congenital abnormalities in 35 children whose mothers had received oral trimethoprim and sulfamethoxazole at the time of conception or shortly thereafter.

Because trimethoprim may interfere with folic acid metabolism, trimethoprim should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nonteratogenic Effects: The oral administration of trimethoprim to rats at a dose of 70 mg/kg/day commencing with the last third of gestation and continuing through parturition and lactation caused no deleterious effects on gestation or pup growth and survival.

Nursing Mothers:

NURSING MOTHERS SECTION

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when polymyxin B sulfate and trimethoprim ophthalmic solution is administered to a nursing woman.

Pediatric Use:

PEDIATRIC USE SECTION

Safety and effectiveness in children below the age of 2 months have not been established (see

WARNINGS).

Geriatric Use:

GERIATRIC USE SECTION

No overall differences in safety or effectiveness have been observed between elderly and other adult patients.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

The most frequent adverse reaction to polymyxin B sulfate and trimethoprim ophthalmic solution is local irritation consisting of increased redness, burning, stinging, and/or itching. This may occur on instillation, within 48 hours, or at any time with extended use. There are also multiple reports of hypersensitivity reactions consisting of lid edema, itching, increased redness, tearing, and/or circumocular rash. Photosensitivity has been reported in patients taking oral trimethoprim.

To report SUSPECTED ADVERSE REACTIONS, contact Somerset Therapeutics, LLC at 1-800-417-9175 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

In mild to moderate infections, instill one drop in the affected eye(s) every three hours (maximum of 6 doses per day) for a period of 7 to 10 days.

HOW SUPPLIED

HOW SUPPLIED SECTION

Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, USP is supplied sterile in natural low density polyethylene (LDPE) ophthalmic bottles and natural low density polyethylene (LDPE) nozzle with white high density polyethylene (HDPE) caps as follows:

10 mL in 10 mL bottle - NDC 70069-311-01

Note: Store at 15° to 25°C (59° to 77°F) and protect from light.

Rx only

For Product Inquiry call +1-800-417-9175

Revised: May, 2024

Manufactured for:

Somerset Therapeutics, LLC.

Somerset, NJ 08873

Made in India

Code No.: KR/DRUGS/KTK/28/289/97

ST-PST11/P/01

1200824

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Container Label (10 mL)

container label
container label

Carton Label

carton label
carton label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
244967polymyxin B sulfate 10,000 UNT / trimethoprim sulfate 1 MG in ML Ophthalmic SolutionPSN5
244967polymyxin B 10000 UNT/ML / trimethoprim 1 MG/ML Ophthalmic SolutionSCD5
244967polymyxin B 10,000 UNT / trimethoprim (as trimethoprim sulfate) 0.1 % Ophthalmic SolutionSY5
244967polymyxin B 10,000 UNT / trimethoprim 0.1 % Ophthalmic SolutionSY5
244967Polymyxin B 10000 UNT/ML / TMP 1 MG/ML Ophthalmic SolutionSY5

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
POLYMYXIN B Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
TRIMETHOPRIM Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4ce811b5-329e-27f8-b5ff-66d52b435c00Product name320240108
8d30c4f0-0228-cea4-e3aa-f19064c47f27Product name320221128
6e20c430-5e8f-85da-1b03-f7dbc0c51fadProduct name320190926
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
c1381fd7-868a-f499-ef90-8f6d3e3ee6b3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70069-311-01polymyxin b sulfate and trimethoprim sulfate10 mL in 1 BOTTLESOLUTION/ DROPS105
70069-311-01polymyxin b sulfate and trimethoprim sulfate1 in 1 CARTONSOLUTION/ DROPS15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70069-311POLYMYXIN B SULFATE AND TRIMETHOPRIM SULFATE SOLUTION/ DROPS [SOMERSET THERAPEUTICS, LLC]5Current NDC, 2 package rows20240808_93d52a75-9a96-4f96-be41-9ccdcabc0933.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70069-311-01ML - Milliliter70069-31197a5f8ef-5487-4636-92b6-db36f09fc31612024-09-09

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70069-31170069-311-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATEPOLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 1 matching rows.

Application-product, TE code table
Application-productTE code
A211572-001AT

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-0584e616aacf4f…
2026-08-18 06:07:402026-07A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-0531067a03dcf5…
2025-08-23 18:47 UTC2025-08A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-056a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-0503ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-052680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-055bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-0579d66fd596c7…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A211572-001TRIMETHOPRIM SULFATE AND POLYMYXIN B SULFATE10,000 UNITS/ML;EQ 1MG BASE/MLSOLUTION/DROPS / OPHTHALMICAT2024-08-05a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A211572-001AT184e616aacf4f…
2026-08-18 06:07:402026-07A211572-001AT1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A211572-001AT1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A211572-001AT131067a03dcf5…
2025-08-23 18:47 UTC2025-08A211572-001AT16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A211572-001AT1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A211572-001AT1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A211572-001AT103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A211572-001AT12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A211572-001AT15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A211572-001AT1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A211572-001AT1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A211572-001AT179d66fd596c7…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A211572-001AT1a50c72e98297…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
polymyxin b sulfate and trimethoprim sulfatePOLYMYXIN B SULFATE AND TRIMETHOPRIM SULFATESomerset Therapeutics, LLC93d52a75-9a96-4f96-be41-9ccdcabc09332024-08-06Warnings, Adverse reactionsExact identifier
ndc (package): 70069-311-01
ndc (product): 70069-311
ndc11 (package): 70069031101
spl id: 80ad4adc-72c3-4398-a639-3d6a6ae9ec17
spl set id: 93d52a75-9a96-4f96-be41-9ccdcabc0933

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.