Neomycin and Polymyxin B Sulfates and Bacitracin Zinc

Manufacturer
Rising Pharma Holdings, Inc. | Jubilant HollisterStier General Partnership
Effective date
2021-11-15
Label type
Human Prescription Drug Label
Version
1
Source
full-release
Hydrated at
2026-05-31 20:38:22

Label at a glance#

ProductNeomycin and Polymyxin B Sulfates and Bacitracin Zinc
Active ingredientNEOMYCIN SULFATE, POLYMYXIN B SULFATE, BACITRACIN ZINC
Label structure10 sections

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Neomycin and Polymyxin B Sulfates and Bacitracin Zinc Ophthalmic Ointment, USP is a sterile antimicrobial ointment for topical ophthalmic use. Each gram contains: neomycin sulfate equivalent to 3.5 mg neomycin base, polymyxin B sulfate equivalent to 10,000 polymyxin B units, and bacitracin zinc equivalent to 400 bacitracin units and petrolatum q.s.

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 of not less than 600 micrograms of neomycin standard per mg, calculated on an anhydrous basis. The structural formulae are:
 


image-1
image-1

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:



image-2
image-2

Bacitracin zinc is the zinc salt of bacitracin, a mixture of related cyclic polypeptides (mainly bacitracin A) produced by the growth of an organism of the licheniformis group of Bacillus subtilis var Tracy. It has a potency of not less than 40 bacitracin units per mg. The structural formula is:



image-3
image-3

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

A wide range of antibacterial action is provided by the overlapping spectra of neomycin, polymyxin B sulfate, and bacitracin.

Neomycin is bactericidal for many gram-positive and gram-negative organisms. It is an aminoglycoside antibiotic which inhibits protein synthesis by binding with ribosomal RNA and causing misreading of the bacterial genetic code.

Polymyxin B is bactericidal for a variety of gram-negative organisms. It increases the permeability of the bacterial cell membrane by interacting with the phospholipid components of the membrane.


Bacitracin is bactericidal for a variety of gram-positive and gram-negative organisms. It interferes with bacterial cell wall synthesis by inhibition of the regeneration of phospholipid receptors involved in peptidoglycan synthesis.

Microbiology

Neomycin sulfate, polymyxin B sulfate and bacitracin zinc together are considered active against the following microorganisms: Staphylococcus aureus, streptococci including Streptococcus pneumoniae, Escherichia coli, Haemophilus influenzae, Klebsiella/Enterobacter species, Neisseria species, and Pseudomonas aeruginosa. The product does not provide adequate coverage against Serratia marcescens.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment is indicated for the topical treatment of superficial infections of the external eye and its adnexa caused by susceptible bacteria. Such infections encompass conjunctivitis, keratitis and keratoconjunctivitis, blepharitis and blepharoconjunctivitis.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment is contraindicated in individuals who have shown hypersensitivity to any of its components.

WARNINGS

WARNINGS SECTION

NOT FOR INJECTION INTO THE EYE. Neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment should never be directly introduced into the anterior chamber of the eye. Ophthalmic ointments may retard corneal wound healing.

Topical antibiotics, particularly neomycin sulfate, may cause cutaneous sensitization. A precise incidence of hypersensitivity reactions (primarily skin rash) due to topical antibiotics is not known. The manifestations of sensitization to topical antibiotics are usually itching, reddening, and edema of the conjunctiva and eyelid. A sensitization reaction may manifest simply as a failure to heal. During long-term use of topical antibiotic products, periodic examination for such signs is advisable, and the patient should be told to discontinue the product if they are observed. Symptoms usually subside quickly on withdrawing the medication. Application of products containing these ingredients should be avoided for the patient thereafter (see PRECAUTIONS: General).

PRECAUTIONS

PRECAUTIONS SECTION

GENERAL

SPL UNCLASSIFIED SECTION

As with other antibiotic preparations, prolonged use of neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment may result in overgrowth of nonsusceptible organisms including fungi. If superinfection occurs, appropriate measures should be initiated.

Bacterial resistance to neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment may also develop. If purulent discharge, inflammation, or pain becomes aggravated, the patient should discontinue use of the medication and consult a physician.

There have been reports of bacterial keratitis associated with the use of topical ophthalmic products in multiple-dose containers which have been inadvertently contaminated by patients, most of whom had a concurrent corneal disease or a disruption of the ocular epithelial surface (see PRECAUTIONS: Information for Patients).

Allergic cross-reactions may occur which could prevent the use of any or all of the following antibiotics for the treatment of future infections: kanamycin, paromomycin, streptomycin, and possibly gentamicin.

INFORMATION FOR PATIENTS

INFORMATION FOR PATIENTS SECTION

Patients should be instructed to avoid allowing the tip of the dispensing container to contact the eye, eyelid, fingers, or any other surface. The use of this product by more than one person may spread infection.

Patients should also be instructed that ocular products, if handled improperly, can become contaminated by common bacteria known to cause ocular infections. Serious damage to the eye and subsequent loss of vision may result from using contaminated products (see PRECAUTIONS: General).

If the condition persists or gets worse, or if a rash or allergic reaction develops, the patient should be advised to stop use and consult a physician. Do not use this product if you are allergic to any of the listed ingredients.

Keep 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 or bacitracin. 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. No adverse effects on male or female fertility, litter size or survival were observed in rabbits given bacitracin zinc 100 gm/ton of diet.

PREGNANCY

PREGNANCY SECTION

Teratogenic Effects: Animal reproduction studies have not been conducted with neomycin sulfate, polymyxin B sulfate, or bacitracin. It is also not known whether neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment should be given to a pregnant woman only if clearly needed.

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 neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment is administered to a nursing woman.

PEDIATRIC USE

PEDIATRIC USE SECTION

Safety and effectiveness in children 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 the anti-infective components of neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment. The exact incidence is not known. Reactions occurring most often are allergic sensitization reactions including itching, swelling, and conjunctival erythema (see WARNINGS). More serious hypersensitivity reactions, including anaphylaxis, have been reported rarely.

Local irritation on instillation has also been reported.

To report SUSPECTED ADVERSE REACTIONS, contact Rising Pharma Holdings, Inc. at (1-844-874-7464) or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Apply the ointment topically into the conjunctival sac of the affected eye(s) every 3 or 4 hours for 7 to 10 days, depending on the severity of the infection.

HOW SUPPLIED

HOW SUPPLIED SECTION

Neomycin and Polymyxin B Sulfates and Bacitracin Zinc Ophthalmic Ointment, USP is supplied in a tube of 1/8 oz (3.5 g) with an ophthalmic tip (NDC 16571-754-53).

Caution: Federal law prohibits dispensing without a prescription.

Store at 15°C to 25°C (59°F to 77°F).

FOR TOPICAL OPHTHALMIC USE

Distributed by:
Rising Pharma Holdings, Inc.
East Brunswick, NJ 08816

Issued: 02/2021

PIA75453-00

Made in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rising®           NDC 16571-754-53

Neomycin and Polymyxin B Sulfates and
Bacitracin Zinc Ophthalmic Ointment, USP

Net wt. 1/8 oz. (3.5g)

Sterile              Rx Only



carton
carton

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
99e684e6-f435-feb8-d2bb-3a546f1cb768Product name220161117
25340b3b-3e4c-4ff8-abf6-3e62ec46bd0cProduct name120160603
2d352c73-a357-4193-a4de-dfdf9a2ac8e4Product name120150819
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
b6082387-f592-1148-0844-bd068fd213fbProduct name120140508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
16571-754NEOMYCIN AND POLYMYXIN B SULFATES AND BACITRACIN ZINC OINTMENT [RISING PHARMA HOLDINGS, INC.]1Legacy NDC20211117_48173c90-79ed-459d-b259-947bc7952c13.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16571-754-53GM - Gram16571-754cafe3402-a8f4-4adc-bd88-219b8c236c7812021-12-08

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
16571-75416571-754-53

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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 44.

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
N050417-001LUMI-SPORYNBACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, 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
N050417-001AT

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 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-10-15 13:18:302026-09N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982c2088c7a36db…
2026-09-14 22:38:342026-08N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 198284e616aacf4f…
2026-08-18 06:07:402026-07N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 198231067a03dcf5…
2025-08-23 18:47 UTC2025-08N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19826a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050417-001LUMI-SPORYN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 198203ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19822680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19825bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 198279d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19821e350fbaab3a…
2024-05-31 18:47 UTC2024-05N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19828072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19825c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GMOINTMENT / OPHTHALMICATRLD, Approved before 19825d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GMOINTMENT / OPHTHALMICATRLD, Approved before 19824b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N050417-001NEOSPORIN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 198274a2ff9319b5…
2022-03-09 01:35 UTC2022-03N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 198287673890dc5c…
2021-03-12 10:30 UTC2021-03N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19825aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19828869cabd3fbd…
2020-11-12 02:37 UTC2020-11N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982c0c555d07b60…
2019-12-14 00:12 UTC2019-12N050417-001NEOSPORIN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19823f01610625f2…
2019-09-15 20:21 UTC2019-09N050417-001NEOSPORIN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982b00525d2431f…
2019-07-19 19:46 UTC2019-07N050417-001NEOSPORIN400 UNITS/GM;EQ 3.5MG BASE/GM;10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19826a51e52b5d6a…
2024-02-18 07:12 UTC2024-02N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19821c564ffb4f44…
2023-12-20 04:57 UTC2023-12N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19829b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19823f0d92c62455…
2023-05-13 08:27 UTC2023-05N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 1982053a50430f4f…
2023-01-26 05:58 UTC2023-01N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19823bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11N050417-001LUMI-SPORYNEQ 400 UNITS/GM;EQ 3.5MG BASE/GM;EQ 10,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for s or e reasons**OINTMENT / OPHTHALMICATRLD, Approved before 19823a93d1ddd44b…

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-10-15 13:18:302026-09N050417-001AT1c2088c7a36db…
2026-09-14 22:38:342026-08N050417-001AT184e616aacf4f…
2026-08-18 06:07:402026-07N050417-001AT1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N050417-001AT1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N050417-001AT131067a03dcf5…
2025-08-23 18:47 UTC2025-08N050417-001AT16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N050417-001AT1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N050417-001AT1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N050417-001AT103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N050417-001AT12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N050417-001AT15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N050417-001AT1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N050417-001AT1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N050417-001AT179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N050417-001AT1301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N050417-001AT11e350fbaab3a…
2024-05-31 18:47 UTC2024-05N050417-001AT18072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N050417-001AT15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N050417-001AT15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N050417-001AT14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N050417-001AT174a2ff9319b5…
2022-03-09 01:35 UTC2022-03N050417-001AT1bb7c543d1eb4…
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2024-02-18 07:12 UTC2024-02N050417-001AT11c564ffb4f44…
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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
746eb2c9-3bcf-4c15-bf7e-2554771d4f4b48173c90-79ed-459d-b259-947bc7952c132025-11-11Warnings, Adverse reactionsExact identifier
spl set id: 48173c90-79ed-459d-b259-947bc7952c13

Reported adverse events (FAERS/openFDA)#

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