Neomycin Polymyxin B Sulfates and Dexamethasone

Manufacturer
MWI/VetOne | Bausch & Lomb Incorporated
Effective date
2010-11-03
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:03

Label at a glance#

ProductNeomycin Polymyxin B Sulfates and Dexamethasone
Active ingredientNeomycin Sulfate, Polymyxin B Sulfate, Dexamethasone
Label structure11 sections

Indications and uses

For steroid-responsive inflammatory ocular conditions for which a corticosteroid is indicated and where bacterial infection or a risk of bacterial ocular infection exists. Ocular steroids are indicated in inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe where the inherent risk of steroid use in certain infective conjunctivitis is accepted to obtain a diminu...

Dosage and administration

One or two drops topically in the conjunctival sac(s). In severe disease, drops may be used hourly, being tapered to discontinuation as the inflammation subsides. In mild disease, drops may be used up to four to six times daily. Not more than 20 mL should be prescribed initially and the prescription should not be refilled without further evaluation as outlined in PRECAUTIONS above. SHAKE WELL BEFORE USING.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Rx only

DESCRIPTION:

DESCRIPTION SECTION

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension USP is a multiple dose anti-infective steroid combination in a sterile suspension for topical application. The active ingredient, Dexamethasone, is represented by the following structural formula:

Dexamethasone (structural formula)
Dexamethasone (structural formula)

C22H29FO5

Mol. Wt. 392.47

Chemical Name: Pregna-1,4-diene-3,20-dione, 9-fluoro-11,17,21-trihydroxy-16-methyl-, (11β,16α)-.

Neomycin Sulfate is the sulfate salt of neomycin B and C which are produced by the growth of Streptomyces fradiae Waksman (Fam. Streptomycetaceae). It has a potency equivalent to not less than 600 micrograms of neomycin base per milligram, calculated on an anhydrous basis. The structural formula is:

Neomycin Sulfate (structural formula)
Neomycin Sulfate (structural formula)

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 milligram, calculated on an anhydrous basis. The structural formula is:

Polymyxin B Sulfate (structural formula)
Polymyxin B Sulfate (structural formula)

Each mL Contains: ACTIVES: Neomycin Sulfate (equivalent to 3.5 mg Neomycin), Polymyxin B Sulfate equal to 10,000 polymyxin B units, Dexamethasone 1 mg (0.1%); INACTIVES: Sodium Chloride, Hypromellose, Polysorbate 20, Purified Water. Hydrochloric Acid and/or Sodium Hydroxide may be added to adjust pH (3.5 – 6.0).
PRESERVATIVE ADDED: Benzalkonium Chloride 0.004%

CLINICAL PHARMACOLOGY:

CLINICAL PHARMACOLOGY SECTION

Corticoids suppress the inflammatory response to a variety of agents and they probably delay or slow the healing. Since corticoids may inhibit the body’s defense mechanism against infection, a concomitant antimicrobial drug may be used when this inhibition is considered to be clinically significant in a particular case.

When a decision to administer both a corticoid and an antimicrobial is made, the administration of such drugs in combination has the advantage of greater patient compliance and convenience, with the added assurance that the appropriate dosage of both drugs is administered, plus assured compatibility of ingredients when both types of drugs are in the same formulation and, particularly, that the correct volume of drug is delivered and retained.

The relative potency of corticosteroids depends on the molecular structure, concentration, and release from the vehicle.

INDICATIONS AND USAGE:

INDICATIONS & USAGE SECTION

For steroid-responsive inflammatory ocular conditions for which a corticosteroid is indicated and where bacterial infection or a risk of bacterial ocular infection exists.

Ocular steroids are indicated in inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe where the inherent risk of steroid use in certain infective conjunctivitis is accepted to obtain a diminution in edema and inflammation. They are also indicated in chronic anterior uveitis and corneal injury from chemical, radiation or thermal burns, or penetration of foreign bodies.

The use of a combination drug with an anti-infective component is indicated where the risk of infection is high or where there is an expectation that potentially dangerous numbers of bacteria will be present in the eye.

The particular anti-infective drug in this product is active against the following common bacterial eye pathogens: Staphylococcus aureus, Escherichia coli, Haemophilus influenzae, Klebsiella/Enterobacter species, Neisseria species, Pseudomonas aeruginosa.

This product does not provide adequate coverage against Serratia marcescens, and Streptococci, including Streptococcus pneumoniae.

CONTRAINDICATIONS:

CONTRAINDICATIONS SECTION

Neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension is contraindicated in most viral diseases of the cornea and conjunctiva, including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. Neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension is also contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids.

WARNINGS:

WARNINGS SECTION

Prolonged use of corticosteroids may result in glaucoma with damage to the optic nerve, defects in visual acuity and fields of vision, and in posterior subcapsular cataract formation. Prolonged use may also suppress the host immune response and thus increase the hazard of secondary ocular infections.

Various ocular diseases and long-term use of topical corticosteroids have been known to cause corneal and scleral thinning. Use of topical corticosteroids in the presence of thin corneal or scleral tissue may lead to perforation.

Acute purulent infections of the eye may be masked or activity enhanced by the presence of corticosteroid medication.

If this product is used for 10 days or longer, intraocular pressure should be routinely monitored even though it may be difficult in children and uncooperative patients. Steroids should be used with caution in the presence of glaucoma. Intraocular pressure should be checked frequently.

The use of steroids after cataract surgery may delay healing and increase the incidence of bleb formation.

Use of ocular steroids may prolong the course and may exacerbate the severity of many viral infections of the eye (including herpes simplex). Employment of a corticosteroid medication in the treatment of patients with a history of herpes simplex requires great caution; frequent slit lamp microscopy is recommended.

Neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension is not for injection. It should never be injected subconjunctivally, nor should it be directly introduced into the anterior chamber of the eye.

Products containing neomycin sulfate may cause cutaneous sensitization.

PRECAUTIONS:

PRECAUTIONS SECTION

General

GENERAL PRECAUTIONS SECTION

The initial prescription and renewal of the medication order beyond 20 mL should be made by a physician only after examination of the patient with the aid of magnification, such as a slit lamp biomicroscopy and, where appropriate, fluorescein staining. If signs and symptoms fail to improve after two days, the patient should be re-evaluated.

As fungal infections of the cornea are particularly prone to develop coincidentally with long-term corticosteroid applications, fungal invasion should be suspected in any persistent corneal ulceration where a corticosteroid has been used or is in use. Fungal cultures should be taken when appropriate.

If this product is used for 10 days or longer, intraocular pressure should be monitored (see WARNINGS).

Prolonged use of topical anti-bacterial agents may give rise to overgrowth of nonsusceptible organisms including fungi.

Information for Patients:

INFORMATION FOR PATIENTS SECTION

If inflammation or pain persists longer than 48 hours or becomes aggravated, the patient should be advised to discontinue use of the medication and consult a physician.

This product is sterile when packaged. To prevent contamination, care should be taken to avoid touching the bottle tip to eyelids or to any other surface. The use of this bottle by more than one person may spread infection. Keep bottle tightly closed when not in use. Keep out of reach of children.

Carcinogenesis, Mutagenesis, Impairment of Fertility

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION

Long-term studies in animals to evaluate carcinogenic or mutagenic potential have not been conducted with polymyxin B sulfate. Treatment of cultured human lymphocytes in vitro with neomycin increased the frequency of chromosome aberrations at the highest concentration (80 µg/mL) tested. However, the effects of neomycin on carcinogenesis and mutagenesis in humans are unknown.

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

Pregnancy

PREGNANCY SECTION

Teratogenic Effects: Pregnancy Category C.

Dexamethasone has been shown to be teratogenic in mice and rabbits following topical ophthalmic application in multiples of the therapeutic dose.

In the mouse, corticosteroids produce fetal resorptions and a specific abnormality, cleft palate. In the rabbit, corticosteroids have produced fetal resorptions and multiple abnormalities involving the head, ears, limbs, palate, etc.

There are no adequate or well-controlled studies in pregnant women. Neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension should be used during pregnancy only if the potential benefit to the mother justifies the potential risk to the embryo or fetus. Infants born of mothers who have received substantial doses of corticosteroids during pregnancy should be observed carefully for signs of hypoadrenalism.

Nursing Mothers

NURSING MOTHERS SECTION

Systemically administered corticosteroids appear in human milk and could suppress growth, interfere with endogenous corticosteroid production, or cause other untoward effects. It is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in human milk. Because many drugs are excreted in human milk, caution should be exercised when neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension is administered to a nursing woman.

Pediatric Use

PEDIATRIC USE SECTION

Safety and effectiveness in pediatric patients below the age of 2 years have not been established.

Geriatric Use

GERIATRIC USE SECTION

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

ADVERSE REACTIONS:

ADVERSE REACTIONS SECTION

Adverse reactions have occurred with steroid/anti-infective combination drugs which can be attributed to the steroid component, the antiinfective component, or the combination. Exact incidence figures are not available since no denominator of treated patients is available.

Reactions occurring most often from the presence of the anti-infective ingredients are allergic sensitizations. The reactions due to the steroid component are: elevation of intraocular pressure (IOP) with possible development of glaucoma, and infrequent optic nerve damage; posterior subcapsular cataract formation; and delayed wound healing.

Corticosteroid-containing preparations have also been reported to cause perforation of the globe. Keratitis, conjunctivitis, corneal ulcers, and conjunctival hyperemia have occasionally been reported following use of steroids.

DOSAGE AND ADMINISTRATION:

DOSAGE & ADMINISTRATION SECTION

One or two drops topically in the conjunctival sac(s). In severe disease, drops may be used hourly, being tapered to discontinuation as the inflammation subsides. In mild disease, drops may be used up to four to six times daily.

Not more than 20 mL should be prescribed initially and the prescription should not be refilled without further evaluation as outlined in PRECAUTIONS above.

SHAKE WELL BEFORE USING.

HOW SUPPLIED:

HOW SUPPLIED SECTION

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension USP is supplied in a controlled drop tip bottle in the following size:

5 mL - Prod. No. 04107

DO NOT USE IF IMPRINTED NECKBAND IS NOT INTACT.

FOR OPHTHALMIC USE ONLY

Storage

STORAGE AND HANDLING SECTION

Store between 15°-30° C (59°-86° F). Store upright.

KEEP OUT OF REACH OF CHILDREN.

Revised September 2008

Bausch & Lomb Incorporated
Tampa, FL 33637
©Bausch & Lomb Incorporated

9114201 (Folded)
9114301 (Flat)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension USP (Carton, 5 mL - MWI)
Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension USP (Carton, 5 mL - MWI)

NDC 13985-028-60

Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension USP

STERILE

Rx only

apexa

5mL

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DexamethasoneACTIVE INGREDIENT7S5I7G3JQL1
Neomycin SulfateACTIVE INGREDIENT057Y6266931
Polymyxin B SulfateACTIVE INGREDIENT19371312D41
DEXAMETHASONEACTIVE MOIETY7S5I7G3JQL1
NEOMYCINACTIVE MOIETYI16QD7X2971
POLYMYXIN BACTIVE MOIETYJ2VZ07J96K1
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W71
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CB1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WO1
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YH1
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8X1
Sodium HydroxideINACTIVE INGREDIENT55X04QC32I1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13985-02813985-028-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 9 · 535 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRA-ARTICULAR26 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOAP / TOPICAL1.26 %w/wExact identifier — unii candidate
134 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHCREAM / TOPICAL108 mgExact identifier — unii candidate
28 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ISOLUTION/ DROPS / OPHTHALMICADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ISOLUTION / DENTALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, SUSPENSION / INTRAMUSCULARADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION / URETHRALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IGEL / TOPICAL70 mgExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ILOTION, AUGMENTED / TOPICALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBSPONGE / TOPICALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRA-ARTERIAL278 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRATHECALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ISOLUTION / TOPICAL39 mgExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBSUSPENSION/ DROPS / TOPICALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYPROMELLOSESHYPROMELLOSE3NXW29V3WOGRANULE, FOR SUSPENSION / ORAL1.7 mgExact identifier — unii candidate
27 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHTABLET, EXTENDED RELEASE / ORAL4.2 mgExact identifier — unii candidate
28 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION / INTRAMUSCULAR176 mgExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRAPERITONEALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION, SUSPENSION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SOLUTION / PARENTERALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ISOLUTION / IRRIGATIONADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBSOLUTION/ DROPS / AURICULAR (OTIC)ADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SOLUTION / INTRATHECAL1.35 mgExact identifier — unii candidate
134 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION / ENDOTRACHEALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SOLUTION / INTRATUMORADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION, SUSPENSION / INTRASYNOVIALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYPROMELLOSESHYPROMELLOSE3NXW29V3WOTABLET, ORALLY DISINTEGRATING / ORAL41 mgExact identifier — unii candidate
27 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION / INTRABURSAL9 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, SOLUTION / SUBCUTANEOUS1486 mgExact identifier — unii candidate
134 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRACARDIACADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINJECTION, EMULSION / INTRAVENOUS0.62 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION / INTRACAUDALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRAVASCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / IONTOPHORESIS0.6 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
HYPROMELLOSESHYPROMELLOSE3NXW29V3WOCAPSULE, EXTENDED RELEASE / ORAL119.7 mgExact identifier — unii candidate
27 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ISOLUTION / NASAL20 mgExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBTABLET, FILM COATED / ORALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBSPRAY / RESPIRATORY (INHALATION)ADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSUSPENSION / ENDOTRACHEAL7.6 mgExact identifier — unii candidate
134 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION, SOLUTION / INTRAVASCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBINJECTION, SOLUTION / INTRAMUSCULAR1037 mgExact identifier — unii candidate
148 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IGEL / TRANSDERMAL472 mgExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ISUSPENSION / AURICULAR (OTIC)ADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IGRANULE, FOR SUSPENSION / ORALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XTABLET, DELAYED RELEASE / ORAL97 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION / PERINEURALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7INJECTION / INTRA-ARTICULAR1 mgExact identifier — unii candidate
24 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IGEL, METERED / TRANSDERMAL350 mgExact identifier — unii candidate
174 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHAEROSOL, FOAM / VAGINAL3 %w/wExact identifier — unii candidate
28 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XINHALANT / RESPIRATORY (INHALATION)3 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, SUSPENSION / SOFT TISSUEADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHSUPPOSITORY / VAGINALNAExact identifier — unii candidate
28 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7SOLUTION/ DROPS / TOPICAL0.01 %w/vExact identifier — unii candidate
24 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSOLUTION / AURICULAR (OTIC)18 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32ILIQUID / INTRAMUSCULARADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium ChlorideSODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / AURICULAR (OTIC)3 mgExact identifier — unii candidate
134 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRATHECALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Sodium HydroxideSODIUM HYDROXIDE55X04QC32IINJECTION, SUSPENSION / INTRALESIONALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
Hydrochloric AcidHYDROCHLORIC ACIDQTT17582CBAEROSOL, METERED / RESPIRATORY (INHALATION)0.7 %w/wExact identifier — unii candidate
148 equally ranked IID candidates

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
A064135-001DEXASPORINDEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13

Therapeutic equivalence codes#

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

Application-product, TE code table
Application-productTE code
A064135-001AT

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.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-1384e616aacf4f…
2026-08-18 06:07:402026-07A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-1331067a03dcf5…
2025-08-23 18:47 UTC2025-08A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-136a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-1303ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-132680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-135bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-1379d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-131e350fbaab3a…
2024-05-31 18:47 UTC2024-05A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-138072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-135c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-135d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-134b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-1374a2ff9319b5…
2022-03-09 01:35 UTC2022-03A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-1387673890dc5c…
2021-03-12 10:30 UTC2021-03A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-135aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-138869cabd3fbd…
2020-11-12 02:37 UTC2020-11A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13c0c555d07b60…
2019-12-14 00:12 UTC2019-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-133f01610625f2…
2019-09-15 20:21 UTC2019-09A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13b00525d2431f…
2019-07-19 19:46 UTC2019-07A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-136a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-131c564ffb4f44…
2023-12-20 04:57 UTC2023-12A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-139b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-133f0d92c62455…
2023-05-13 08:27 UTC2023-05A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13053a50430f4f…
2023-01-26 05:58 UTC2023-01A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-133bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-133a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A064135-001DEXASPORIN0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICAT1995-09-13f41ea6bd6efb…

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A064135-001AT184e616aacf4f…
2026-08-18 06:07:402026-07A064135-001AT1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A064135-001AT1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A064135-001AT131067a03dcf5…
2025-08-23 18:47 UTC2025-08A064135-001AT16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A064135-001AT1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A064135-001AT1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A064135-001AT103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A064135-001AT12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A064135-001AT15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A064135-001AT1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A064135-001AT1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A064135-001AT179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A064135-001AT1301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A064135-001AT11e350fbaab3a…
2024-05-31 18:47 UTC2024-05A064135-001AT18072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A064135-001AT15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A064135-001AT15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A064135-001AT14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A064135-001AT174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A064135-001AT1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A064135-001AT1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A064135-001AT187673890dc5c…
2021-03-12 10:30 UTC2021-03A064135-001AT15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A064135-001AT18869cabd3fbd…
2020-11-12 02:37 UTC2020-11A064135-001AT1c0c555d07b60…
2019-12-14 00:12 UTC2019-12A064135-001AT13f01610625f2…
2019-09-15 20:21 UTC2019-09A064135-001AT1b00525d2431f…
2019-07-19 19:46 UTC2019-07A064135-001AT1ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A064135-001AT16a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A064135-001AT11c564ffb4f44…
2023-12-20 04:57 UTC2023-12A064135-001AT1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A064135-001AT1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A064135-001AT19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A064135-001AT1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A064135-001AT13f0d92c62455…
2023-05-13 08:27 UTC2023-05A064135-001AT1053a50430f4f…
2023-01-26 05:58 UTC2023-01A064135-001AT13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A064135-001AT13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A064135-001AT1f41ea6bd6efb…

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
266c6704-a98b-61af-e063-6394a90a5cd701e58ae0-cdcf-4c1f-bfb9-9d0fc3ebd0022024-11-08Warnings, Adverse reactionsExact identifier
spl set id: 01e58ae0-cdcf-4c1f-bfb9-9d0fc3ebd002

Reported adverse events (FAERS/openFDA)#

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