c7a804bc-dac8-47dc-b7a8-8f2d384652f2 — v1

3 Views

Version

v1

Effective date

August 1, 2009

Original packager

Sections captured

19

Identifiers

Document ID
158f00a6-9a60-40d6-8a7b-08a021c6201b
Set ID
c7a804bc-dac8-47dc-b7a8-8f2d384652f2
Application numbers
Product NDCs
Package NDCs
Original packager NDCs

Names & Manufacturers

Brand names
Generic names
Manufacturer names
Product types

Substances & Pharmacology

Substance names
Routes
Pharmacologic class (PE)
Pharmacologic class (EPC)
Pharmacologic class (CS)
Mechanism of action

Other identifiers

NUI
RxCUI
UNII
UPC

Structured Label Sections

Adverse Reactions (1)

Sequence 1

ADVERSE REACTIONS: The most frequently reported adverse reactions are minor ocular irritations, redness, and hypersensitivity reactions.
Carcinogenesis And Mutagenesis And Impairment Of Fertility (1)

Sequence 1

Carcinogenesis, Mutagenesis, Impairment of Fertility: Two year oral studies conducted in rats with erythromycin did not provide evidence of tumorigenicity. Mutagenicity studies have not been conducted. No evidence of impaired fertility that appeared related to erythromycin was reported in animal studies.
Clinical Pharmacology (1)

Sequence 1

CLINICAL PHARMACOLOGY: Microbiology: Erythromycin inhibits protein synthesis without affecting nucleic acid synthesis. Erythromycin is usually active against the following organisms in vitro and in clinical infections: Streptococcus pyogenes (group A ß-hemolytic) Alpha-hemolytic streptococci (viridans group) Staphylococcus aureus , including penicillinase-producing strains (methicillin-resistant staphylococci are uniformly resistant to erythromycin) Streptococcus pneumoniae Mycoplasma pneumoniae (Eaton Agent, PPLO) Haemophilus influenzae (not all strains of this organism are susceptible at the erythromycin concentrations ordinarily achieved) Treponema pallidum Corynebacterium diphtheriae Neisseria gonorrhoeae Chlamydia trachomatis
Contraindications (1)

Sequence 1

CONTRAINDICATIONS: This drug is contraindicated in patients with a history of hypersensitivity to erythromycin.
Description (1)

Sequence 1

DESCRIPTION: Erythromycin Ophthalmic Ointment belongs to the macrolide group of antibiotics. It is basic and readily forms a salt when combined with an acid. The base, as crystals or powder, is slightly soluble in water, moderately soluble in ether, and readily soluble in alcohol or chloroform. Erythromycin ((3R*,4S*,5S*,6R*,7R*,9R*,11R*,12R*,13S*,14R*)-4-[(2,6-dideoxy-3-C-methyl-3-0-methyl-ɑ-L-ribo-hexopyranosyl)oxy]-14-ethyl-7,12,13-trihydroxy-3,5,7,9,11,13-hexamethyl-6-[[3,4,6-trideoxy-3-(dimethylamino)-ß-D-xylo-hexopyranosyl]oxy] oxacyclotetradecane-2,10-dione) is an antibiotic produced from a strain of Streptomyces erythraeus . It has the following structural formula: Molecular Formula: C 37 H 67 NO 13 Molecular Weight: 733.94 Each gram contains Erythromycin USP 5 mg in a sterile ophthalmic base of mineral oil and white petrolatum. Erythromicin structural formula
Dosage And Administration (1)

Sequence 1

DOSAGE AND ADMINISTRATION: In the treatment of superficial ocular infections, a ribbon approximately 1 cm in length of Erythromycin Ophthalmic Ointment should be applied directly to the infected structure up to 6 times daily, depending on the severity of the infection. For prophylaxis of neonatal gonococcal or chlamydial conjunctivitis, a ribbon of ointment approximately 1 cm in length should be instilled into each lower conjunctival sac. The ointment should not be flushed from the eye following instillation. A new tube should be used for each infant.
General Precautions (1)

Sequence 1

General: The use of antimicrobial agents may be associated with the overgrowth of nonsusceptible organisms including fungi; in such a case, antibiotic administration should be stopped and appropriate measures taken.
How Supplied (1)

Sequence 1

HOW SUPPLIED: Sterile Erythromycin Ophthalmic Ointment USP, 5 mg/g as follows: 3.5 g (1/8 oz) tamper-evident tubes NDC 54868-0644-1 Store at controlled room temperature 15°-30°C (59°-86°F). Avoid excessive heat. Protect from freezing.
Indications And Usage (1)

Sequence 1

INDICATIONS AND USAGE: For the treatment of superficial ocular infections involving the conjunctiva and/or cornea caused by organisms susceptible to erythromycin. For prophylaxis of ophthalmia neonatorum due to N. gonorrhoeae or C. trachomatis . The effectiveness of erythromycin in the prevention of ophthalmia caused by penicillinase-producing N. gonorrhoeae is not established. For infants born to mothers with clinically apparent gonorrhea, intravenous or intramuscular injections of aqueous crystalline penicillin G should be given; a single dose of 50,000 units for term infants or 20,000 units for infants of low birth weight. Topical prophylaxis alone is inadequate for these infants.
Information For Patients (1)

Sequence 1

Information for Patients: Avoid contaminating the applicator tip with material from the eye, fingers, or other source.
Microbiology (1)

Sequence 1

Microbiology: Erythromycin inhibits protein synthesis without affecting nucleic acid synthesis. Erythromycin is usually active against the following organisms in vitro and in clinical infections: Streptococcus pyogenes (group A ß-hemolytic) Alpha-hemolytic streptococci (viridans group) Staphylococcus aureus , including penicillinase-producing strains (methicillin-resistant staphylococci are uniformly resistant to erythromycin) Streptococcus pneumoniae Mycoplasma pneumoniae (Eaton Agent, PPLO) Haemophilus influenzae (not all strains of this organism are susceptible at the erythromycin concentrations ordinarily achieved) Treponema pallidum Corynebacterium diphtheriae Neisseria gonorrhoeae Chlamydia trachomatis
Nursing Mothers (1)

Sequence 1

Nursing Mothers: Caution should be exercised when erythromycin is administered to a nursing woman.
Package Label Principal Display Panel (1)

Sequence 1

PRINCIPAL DISPLAY PANEL - CARTON LABEL 3.5 g (1/8 Oz) Rx only ERYTHROMYCIN OPHTHALMIC OINTMENT USP STERILE USUAL DOSAGE: Apply to the affected area one or more times daily. See insert for complete information. CONTAINS: Erythromycin USP 5 mg per gram in a sterile ophthalmic base of Mineral Oil and White Petrolatum. NET WT 3.5 g (1/8 Oz) STORE AT ROOM TEMPERATURE. AVOID EXCESSIVE HEAT. PROTECT FROM FREEZING. KEEP TIGHTLY CLOSED. WARNING: Keep out of reach of children. Erythromycin Carton Label
Pediatric Use (1)

Sequence 1

Pediatric Use: See INDICATIONS AND USAGE and DOSAGE AND ADMINISTRATION .
Precautions (1)

Sequence 1

PRECAUTIONS: General: The use of antimicrobial agents may be associated with the overgrowth of nonsusceptible organisms including fungi; in such a case, antibiotic administration should be stopped and appropriate measures taken. Information for Patients: Avoid contaminating the applicator tip with material from the eye, fingers, or other source. Carcinogenesis, Mutagenesis, Impairment of Fertility: Two year oral studies conducted in rats with erythromycin did not provide evidence of tumorigenicity. Mutagenicity studies have not been conducted. No evidence of impaired fertility that appeared related to erythromycin was reported in animal studies. Pregnancy: Teratogenic effects Pregnancy category B. Reproduction studies have been performed in rats, mice, and rabbits using erythromycin and its various salts and esters, at doses that were several multiples of the usual human dose. No evidence of harm to the fetus that appeared related to erythromycin was reported in these studies. There are, however, no adequate and well controlled studies in pregnant women. Because animal reproductive studies are not always predictive of human response, the erythromycins should be used during pregnancy only if clearly needed. Nursing Mothers: Caution should be exercised when erythromycin is administered to a nursing woman. Pediatric Use: See INDICATIONS AND USAGE and DOSAGE AND ADMINISTRATION .
Pregnancy (1)

Sequence 1

Pregnancy: Teratogenic effects Pregnancy category B. Reproduction studies have been performed in rats, mice, and rabbits using erythromycin and its various salts and esters, at doses that were several multiples of the usual human dose. No evidence of harm to the fetus that appeared related to erythromycin was reported in these studies. There are, however, no adequate and well controlled studies in pregnant women. Because animal reproductive studies are not always predictive of human response, the erythromycins should be used during pregnancy only if clearly needed.
Spl Product Data Elements (1)

Sequence 1

Erythromycin Erythromycin ERYTHROMYCIN ERYTHROMYCIN MINERAL OIL PETROLATUM
Spl Unclassified Section (2)

Sequence 1

Rx only

Sequence 2

Manufactured for: Fera Pharmaceuticals, LLC Locust Valley, NY 11560 FPEH00N Rev. 09/09 Relabeling of "Additional Barcode" label by: Physicians Total Care, Inc. Tulsa, OK 74146 Fera Logo
Teratogenic Effects (1)

Sequence 1

Teratogenic effects Pregnancy category B. Reproduction studies have been performed in rats, mice, and rabbits using erythromycin and its various salts and esters, at doses that were several multiples of the usual human dose. No evidence of harm to the fetus that appeared related to erythromycin was reported in these studies. There are, however, no adequate and well controlled studies in pregnant women. Because animal reproductive studies are not always predictive of human response, the erythromycins should be used during pregnancy only if clearly needed.