Maxitrol

Manufacturer
Alcon Laboratories, Inc.
Effective date
2021-05-14
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 22:44:21

Label at a glance#

ProductMaxitrol
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 infection exists. Ocular corticosteroids are indicated in inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe where the inherent risk of corticosteroids use in certain infective conjunctivitides is accepted to obtai...

Dosage and administration

One to two drops 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.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

MAXITROL® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension)Sterile

SPL UNCLASSIFIED SECTION

DESCRIPTION

DESCRIPTION SECTION

MAXITROL® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) is a multiple dose anti-infective steroid combination in sterile suspension form for topical application. The chemical structure for the active ingredient, dexamethasone, is:

The chemical structure for the active ingredient, dexamethasoneThe chemical structure for the active ingredient, dexamethasone

C22H29FO5

Established name: dexamethasone

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

The other active ingredients are neomycin sulfate and polymyxin B sulfate. The structural formula for neomycin sulfate is:

The structural formula for neomycin sulfateThe structural formula for neomycin sulfate

Neomycin B (R1=H, R2=CH2NH2)

Neomycin C (R1=CH2NH2, R2=H)

The structural formula for polymyxin B sulfate is:

The structural formula for polymyxin B sulfateThe structural formula for polymyxin B sulfate

Each mL of MAXITROL® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) contains: Actives: neomycin sulfate equivalent to neomycin 3.5 mg, polymyxin B sulfate 10,000 units, dexamethasone 0.1%. Inactives: benzalkonium chloride 0.004% (preservative), hydrochloric acid and/or sodium hydroxide (to adjust pH), hypromellose 2910 0.5%, polysorbate 20, purified water, sodium chloride.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Corticosteroids suppress the inflammatory response to a variety of agents and they probably delay or slow healing. Since corticosteroids 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 corticosteroid 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 infection exists.

Ocular corticosteroids are indicated in inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe where the inherent risk of corticosteroids use in certain infective conjunctivitides 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, and Pseudomonas aeruginosa.

This product does not provide adequate coverage against: Serratia   marces c ens  and streptococci, including Streptococcus pneumoniae.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

MAXITROL® (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. MAXITROL 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

NOT FOR INJECTION. 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.

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

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.

If this product is used for 10 days or longer, intraocular pressure (IOP) 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. IOP should be checked frequently.

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

MAXITROL® (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. Sensitivity to topically administered aminoglycosides, such as neomycin, may occur in some patients. Severity of hypersensitivity reactions may vary from local effects to generalized reactions such as erythema, itching, urticaria, skin rash, anaphylaxis, anaphylactoid reactions, or bullous reactions. If hypersensitivity develops during use of the product, treatment should be discontinued. Cross-hypersensitivity to other aminoglycosides can occur, and the possibility that patients who become sensitized to topical neomycin may also be sensitive to other topical and/or systemic aminoglycosides should be considered.

PRECAUTIONS

PRECAUTIONS SECTION

General

GENERAL PRECAUTIONS SECTION

The initial prescription and renewal of the medication order beyond 20 mL of MAXITROL® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) should be made by a physician only after examination of the patient with the aid of magnification, such as slit lamp biomicroscopy, and where appropriate, fluorescein staining. If signs and symptoms fail to improve after two days, the patient should be reevaluated.

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, IOP should be monitored (see   WARNINGS).

Prolonged use of topical anti-bacterial agents may give rise to overgrowth of non-susceptible 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.

Patients should be advised that their vision may be temporarily blurred following dosing with MAXITROL®  (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension). Care should be exercised in operating machinery or driving a motor vehicle.

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 mcg/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

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. However, prolonged or repeated corticoid use during pregnancy has been associated with an increased risk of intra-uterine growth retardation. MAXITROL® (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, 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 MAXITROL® (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 corticosteroid/anti-infective combination drugs which can be attributed to the corticosteroid component, the anti-infective 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 ingredient are allergic sensitizations. The reactions due to the corticosteroid component are: elevation of 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.

Additional adverse reactions identified from post marketing use include ulcerative keratitis, headache, and Stevens-Johnson syndrome.

The following additional adverse reactions have been reported with dexamethasone use:

Cushing’s syndrome and adrenal suppression may occur after use of dexamethasone in excess of the listed dosing instructions in predisposed patients, including children and patients treated with CYP3A4 inhibitors.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

One to two drops 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.

HOW SUPPLIED

HOW SUPPLIED SECTION

MAXITROL® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) is supplied as a sterile ophthalmic suspension in a white, low density polyethylene dispenser with a pink, polypropylene cap as follows:

5 mL in 8 mL bottle……………………………………………………….NDC 0998-0630-06

Storage: Store upright at 8°C to 27°C (46°F to 80°F).

After opening, MAXITROL (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) can be used until the expiration date on the bottle.

© Novartis

Distributed by:
Novartis Pharmaceuticals Corporation
East Hanover, New Jersey 07936

T2021-61

May 2021

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 0998-0630-06

Alcon®

Maxitrol®

(neomycin and

polymyxin B sulfates

and dexamethasone

ophthalmic

suspension)

5 mL Sterile

NDC 0998-0630-06 Alcon® Maxitrol® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) 5 mL SterileNDC 0998-0630-06 Alcon® Maxitrol® (neomycin and polymyxin B sulfates and dexamethasone ophthalmic suspension) 5 mL Sterile

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0998-0630-062024-05-02C16284748780-1e4f33bdf-a11b-d8a0-e053-dadaa90a6e4e277ff310-b7dc-43b6-8a16-885b58882bc0
0998-0630-062022-07-29C16284748780-1e4f33bdf-a11b-d8a0-e053-dadaa90a6e4e277ff310-b7dc-43b6-8a16-885b58882bc0

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0998-0630-06ML - Milliliter0998-0630c6c36128-f66e-43db-85f4-e5ec0bd415c812012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DEXAMETHASONEACTIVE INGREDIENT7S5I7G3JQL3
NEOMYCIN SULFATEACTIVE INGREDIENT057Y6266933
POLYMYXIN B SULFATEACTIVE INGREDIENT19371312D43
DEXAMETHASONEACTIVE MOIETY7S5I7G3JQL3
NEOMYCINACTIVE MOIETYI16QD7X2973
POLYMYXIN BACTIVE MOIETYJ2VZ07J96K3
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W73
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CB3
HYPROMELLOSE 2910 (4000 MPA.S)INACTIVE INGREDIENTRN3152OP353
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YH3
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8X3
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32I3
WATERINACTIVE INGREDIENT059QF0KO0R3

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
0998-06300998-0630-06

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 · 529 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRASPINALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / INTRA-ARTERIALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBLOTION / TOPICALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRA-AMNIOTICADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ITABLET, DELAYED RELEASE / ORAL4 mgExact identifier — unii candidate
174 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHINJECTION / SUBCUTANEOUSNAExact identifier — unii candidate
28 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAMUSCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, SUSPENSION / INTRASYNOVIAL4 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 HYDROXIDE55X04QC32IPOWDER / INTRAVENOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISYRUP / ORAL71 mg/5mlExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARYADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBTABLET, FILM COATED / ORALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION / TOPICAL0.32 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IDROPS / OPHTHALMICNAExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRACARDIACADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSUSPENSION, EXTENDED RELEASE / ORALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSPRAY, METERED / NASALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYPROMELLOSE 2910 (4000 MPA.S)HYPROMELLOSE 2910 (4000 MPA.S)RN3152OP35TABLET, FOR SUSPENSION / ORAL90 mgExact identifier — unii candidate
21 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ILIQUID / TOPICALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / EPIDURALADJ 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
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / INTRABURSALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, EMULSION / INTRAVENOUSADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHLOTION / TOPICAL2000 mgExact identifier — unii candidate
28 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRAVASCULARADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHINJECTION / INTRAVENOUS30 mgExact identifier — unii candidate
28 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHCREAM / TOPICAL108 mgExact identifier — unii candidate
28 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, FOR SOLUTION / INTRATHECALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISUSPENSION / AURICULAR (OTIC)ADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBDROPS / NASAL10 mlExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ITABLET / ORAL10 mgExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUSADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVERNOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION / INTRAVASCULARADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUSADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / SUBCONJUNCTIVALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBCREAM / TOPICAL38 mgExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, SUSPENSION / SOFT TISSUEADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER, FOR SUSPENSION / ORAL98 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XTABLET, DELAYED RELEASE / ORAL97 mgExact identifier — unii candidate
134 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHTABLET, FILM COATED / ORAL0.35 mgExact identifier — unii candidate
28 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBSOLUTION/ DROPS / TOPICALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION / ENDOTRACHEALADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSUSPENSION/ DROPS / TOPICAL0.23 %w/vExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XCAPSULE / ORAL6 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XPOWDER / RESPIRATORY (INHALATION)NAExact identifier — unii candidate
134 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7SHAMPOO / TOPICAL0.2 %w/wExact identifier — unii candidate
24 equally ranked IID candidates
POLYSORBATE 20POLYSORBATE 207T1F30V5YHINJECTION, SOLUTION / INTRAVENOUS30 mgExact identifier — unii candidate
28 equally ranked IID candidates
HYDROCHLORIC ACIDHYDROCHLORIC ACIDQTT17582CBINJECTION, SOLUTION / INFILTRATIONADJ PHExact identifier — unii candidate
148 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / INTRATHECALADJ 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
POLYSORBATE 20POLYSORBATE 207T1F30V5YHSUSPENSION / ORAL80 mgExact identifier — unii candidate
28 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IOINTMENT, AUGMENTED / TOPICAL0.11 %w/wExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / EXTRACORPOREALADJ PHExact identifier — unii candidate
174 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XINJECTION, POWDER, FOR SUSPENSION / INTRA-ARTICULAR45 mgExact identifier — unii candidate
134 equally ranked IID candidates
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IFILM, EXTENDED RELEASE / TRANSDERMAL0.85 mgExact identifier — unii candidate
174 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
N050023-002MAXITROLDEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982

Therapeutic equivalence codes#

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

Application-product, TE code table
Application-productTE code
N050023-002AT

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 22:38:342026-08N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 198284e616aacf4f…
2026-08-18 06:07:402026-07N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 198231067a03dcf5…
2025-08-23 18:47 UTC2025-08N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19826a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 198203ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19822680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19825bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 198279d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19821e350fbaab3a…
2024-05-31 18:47 UTC2024-05N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19828072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19825c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19825d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19824b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 198274a2ff9319b5…
2022-03-09 01:35 UTC2022-03N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 198287673890dc5c…
2021-03-12 10:30 UTC2021-03N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19825aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19828869cabd3fbd…
2020-11-12 02:37 UTC2020-11N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982c0c555d07b60…
2019-12-14 00:12 UTC2019-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19823f01610625f2…
2019-09-15 20:21 UTC2019-09N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982b00525d2431f…
2019-07-19 19:46 UTC2019-07N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19826a51e52b5d6a…
2024-02-18 07:12 UTC2024-02N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19821c564ffb4f44…
2023-12-20 04:57 UTC2023-12N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19829b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19823f0d92c62455…
2023-05-13 08:27 UTC2023-05N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982053a50430f4f…
2023-01-26 05:58 UTC2023-01N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19823bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 19823a93d1ddd44b…
2022-10-28 04:53 UTC2022-10N050023-002MAXITROL0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/MLSUSPENSION/DROPS / OPHTHALMICATRLD, RS, Approved before 1982f41ea6bd6efb…

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 22:38:342026-08N050023-002AT184e616aacf4f…
2026-08-18 06:07:402026-07N050023-002AT1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N050023-002AT1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050023-002AT131067a03dcf5…
2025-08-23 18:47 UTC2025-08N050023-002AT16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050023-002AT1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050023-002AT1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050023-002AT103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050023-002AT12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050023-002AT15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050023-002AT1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N050023-002AT1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050023-002AT179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050023-002AT1301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050023-002AT11e350fbaab3a…
2024-05-31 18:47 UTC2024-05N050023-002AT18072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050023-002AT15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N050023-002AT15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N050023-002AT14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N050023-002AT174a2ff9319b5…
2022-03-09 01:35 UTC2022-03N050023-002AT1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12N050023-002AT1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N050023-002AT187673890dc5c…
2021-03-12 10:30 UTC2021-03N050023-002AT15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12N050023-002AT18869cabd3fbd…
2020-11-12 02:37 UTC2020-11N050023-002AT1c0c555d07b60…
2019-12-14 00:12 UTC2019-12N050023-002AT13f01610625f2…
2019-09-15 20:21 UTC2019-09N050023-002AT1b00525d2431f…
2019-07-19 19:46 UTC2019-07N050023-002AT1ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03N050023-002AT16a51e52b5d6a…
2024-02-18 07:12 UTC2024-02N050023-002AT11c564ffb4f44…
2023-12-20 04:57 UTC2023-12N050023-002AT1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11N050023-002AT1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10N050023-002AT19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07N050023-002AT1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06N050023-002AT13f0d92c62455…
2023-05-13 08:27 UTC2023-05N050023-002AT1053a50430f4f…
2023-01-26 05:58 UTC2023-01N050023-002AT13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11N050023-002AT13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10N050023-002AT1f41ea6bd6efb…

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
176bbcf9-8ffa-2860-e063-6394a90a5fe4277ff310-b7dc-43b6-8a16-885b58882bc02024-05-01Warnings, Adverse reactionsExact identifier
spl set id: 277ff310-b7dc-43b6-8a16-885b58882bc0

Reported adverse events (FAERS/openFDA)#

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