Indications and uses
CIPRO® HC OTIC is indicated for the treatment of acute otitis externa in adult and pediatric patients, one year and older, due to susceptible strains of Pseudomonas aeruginosa , Staphylococcus aureus , and Proteus mirabilis .
CIPRO® HC OTIC is indicated for the treatment of acute otitis externa in adult and pediatric patients, one year and older, due to susceptible strains of Pseudomonas aeruginosa , Staphylococcus aureus , and Proteus mirabilis .
SHAKE WELL IMMEDIATELY BEFORE USING. For children (age 1 year and older) and adults, 3 drops of the suspension should be instilled into the affected ear twice daily for seven days. The suspension should be warmed by holding the bottle in the hand for 1-2 minutes to avoid the dizziness which may result from the instillation of a cold solution into the ear canal. The patient should lie with the affected ear upward a...
CIPRO® HC OTIC (ciprofloxacin hydrochloride and hydrocortisone otic suspension) contains the synthetic broad spectrum antibacterial agent, ciprofloxacin hydrochloride, combined with the anti-inflammatory corticosteroid, hydrocortisone, in a preserved, nonsterile suspension for otic use. Each mL of CIPRO® HC OTIC contains ciprofloxacin hydrochloride (equivalent to 2 mg ciprofloxacin), 10 mg hydrocortisone, and 9 mg benzyl alcohol as a preservative. The inactive ingredients are polyvinyl alcohol, sodium chloride, sodium acetate, glacial acetic acid, phospholipon 90H (modified lecithin), polysorbate, and purified water. Sodium hydroxide or hydrochloric acid may be added for adjustment of pH.
Ciprofloxacin, a fluoroquinolone, is available as the monohydrochloride monohydrate salt of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid. Its empirical formula is C17H18FN3O3•HCI•H2O and its chemical structure is as follows:

Hydrocortisone, pregn-4-ene-3, 20-dione, 11, 17, 21-trihydroxy-(11(β)-, is an anti-inflammatory corticosteroid. Its empirical formula is C21H30O5 and its chemical structure is:

The plasma concentrations of ciprofloxacin were not measured following three drops of otic suspension administration because the systemic exposure to ciprofloxacin is expected to be below the limit of quantitation of the assay (0.05 μg/mL).
Similarly, the predicted Cmax of hydrocortisone is within the range of endogenous hydrocortisone concentration (0-150 ng/mL), and therefore cannot be differentiated from the endogenous cortisol.
Preclinical studies have shown that CIPRO® HC OTIC was not toxic to the guinea pig cochlea when administered intratympanically twice daily for 30 days and was only weakly irritating to rabbit skin upon repeated exposure.
Hydrocortisone has been added to aid in the resolution of the inflammatory response accompanying bacterial infection.
Microbiology
Ciprofloxacin has in vitro activity against a wide range of gram-positive and gram-negative microorganisms. The bactericidal action of ciprofloxacin results from interference with the enzyme, DNA gyrase, which is needed for the synthesis of bacterial DNA. Cross-resistance has been observed between ciprofloxacin and other fluoroquinolones. There is generally no cross-resistance between ciprofloxacin and other classes of antibacterial agents such as beta-lactams or aminoglycosides.
Ciprofloxacin has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections of acute otitis externa as described in the INDICATIONS AND USAGE section:
Aerobic gram-positive microorganism
Staphylococcus aureus
Aerobic gram-negative microorganisms
Proteus mirabilis
Pseudomonas aeruginosa
CIPRO® HC OTIC is indicated for the treatment of acute otitis externa in adult and pediatric patients, one year and older, due to susceptible strains of Pseudomonas aeruginosa, Staphylococcus aureus, and Proteus mirabilis.
CIPRO® HC OTIC is contraindicated in persons with a history of hypersensitivity to hydrocortisone, ciprofloxacin or any member of the quinolone class of antimicrobial agents. This nonsterile product should not be used if the tympanic membrane is known or suspected to be perforated. Use of this product is contraindicated in viral infections of the external canal including varicella and herpes simplex infections.
NOT FOR OPHTHALMIC USE. NOT FOR INJECTION.
CIPRO® HC OTIC should be discontinued at the first appearance of a skin rash or any other sign of hypersensitivity. Serious and occasionally fatal hypersensitivity (anaphylactic) reactions, some following the first dose, have been reported in patients receiving systemic quinolones. Serious acute hypersensitivity reactions may require immediate emergency treatment. The dropper cap contains natural rubber (latex) which may cause severe allergic reactions.
As with other antibiotic preparations, use of this product may result in overgrowth of nonsusceptible organisms, including fungi. If the infection is not improved after one week of therapy, cultures should be obtained to guide further treatment.
If rash or allergic reaction occurs, discontinue use immediately and contact your physician.
Do not use in the eyes.
Avoid contaminating the dropper with material from the ear, fingers, or other sources.
Protect from light.
Shake well immediately before using.
Discard unused portion after therapy is completed.
Eight in vitro mutagenicity tests have been conducted with ciprofloxacin, and the test results are listed below:
Salmonella/Microsome Test (Negative)
E. coli DNA Repair Assay (Negative)
Mouse Lymphoma Cell Forward Mutation Assay (Positive)
Chinese Hamster V79 Cell HGPRT Test (Negative)
Syrian Hamster Embryo Cell Transformation Assay (Negative)
Saccharomyces cerevisiae Point Mutation Assay (Negative)
Saccharomyces cerevisiae Mitotic Crossover and Gene Conversion Assay (Negative)
Rat Hepatocyte DNA Repair Assay (Positive)
Thus, 2 of the 8 tests were positive, but results of the following 3 in vivo test systems gave negative results:
Rat Hepatocyte DNA Repair Assay
Micronucleus Test (Mice)
Dominant Lethal Test (Mice)
Long-term carcinogenicity studies in mice and rats have been completed for ciprofloxacin. After daily oral doses of 750 mg/kg (mice) and 250 mg/kg (rats) were administered for up to 2 years, there was no evidence that ciprofloxacin had any carcinogenic or tumorigenic effects in these species. No long term studies of CIPRO® HC OTIC suspension have been performed to evaluate carcinogenic potential.
Fertility studies performed in rats at oral doses of ciprofloxacin up to 100 mg/kg/day revealed no evidence of impairment. This would be over 1000 times the maximum recommended clinical dose of ototopical ciprofloxacin based upon body surface area, assuming total absorption of ciprofloxacin from the ear of a patient treated with CIPRO® HC OTIC twice per day.
Long term studies have not been performed to evaluate the carcinogenic potential or the effect on fertility of topical hydrocortisone. Mutagenicity studies with hydrocortisone were negative.
Reproduction studies have been performed in rats and mice using oral doses of up to 100 mg/kg and IV doses up to 30 mg/kg and have revealed no evidence of harm to the fetus as a result of ciprofloxacin. In rabbits, ciprofloxacin (30 and 100 mg/kg orally) produced gastrointestinal disturbances resulting in maternal weight loss and an increased incidence of abortion, but no teratogenicity was observed at either dose. After intravenous administration of doses up to 20 mg/kg, no maternal toxicity was produced in the rabbit, and no embryotoxicity or teratogenicity was observed.
Corticosteroids are generally teratogenic in laboratory animals when administered systemically at relatively low dosage levels. The more potent corticosteroids have been shown to be teratogenic after dermal application in laboratory animals.
Animal reproduction studies have not been conducted with CIPRO® HC OTIC. No adequate and well controlled studies have been performed in pregnant women. Caution should be exercised when CIPRO® HC OTIC is used by a pregnant woman.
Ciprofloxacin is excreted in human milk with systemic use. It is not known whether ciprofloxacin is excreted in human milk following topical otic administration. Because of the potential for serious adverse reactions in nursing infants, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
The safety and efficacy of CIPRO® HC OTIC have been established in pediatric patients 2 years and older (131 patients) in adequate and well-controlled clinical trials. Efficacy has been extrapolated for patients, age 1 year and above based on studies in adults and older pediatric patients.
In Phase 3 clinical trials, a total of 564 patients were treated with CIPRO® HC OTIC. Adverse events with at least remote relationship to treatment included headache (1.2%) and pruritus (0.4%). The following treatment-related adverse events were each reported in a single patient: migraine, hypesthesia, paresthesia, fungal dermatitis, cough, rash, urticaria, and alopecia.
The following reactions have been identified during post-approval use of CIPRO® HC OTIC in clinical practice. Because they are reported voluntarily from a population of unknown size, estimates of frequency cannot be made. The reactions, which have been chosen for inclusion due to either their seriousness, frequency of reporting, possible causal connection to CIPRO® HC OTIC, or a combination of these factors, include: dizziness, ear canal erythema, ear congestion, hypoacusis and medication residue.
SHAKE WELL IMMEDIATELY BEFORE USING.
For children (age 1 year and older) and adults, 3 drops of the suspension should be instilled into the affected ear twice daily for seven days. The suspension should be warmed by holding the bottle in the hand for 1-2 minutes to avoid the dizziness which may result from the instillation of a cold solution into the ear canal. The patient should lie with the affected ear upward and then the drops should be instilled. This position should be maintained for 30-60 seconds to facilitate penetration of the drops into the ear. Repeat, if necessary, for the opposite ear. Discard unused portion after therapy is completed.
CIPRO® HC OTIC is supplied as a white to off-white opaque suspension in a 10 mL bottle with a dropper dispenser.
NDC 0065-8531-10
Store below 77° F (25° C). Avoid freezing. Protect from light.
U.S. Pat.:
www.alconpatents.com
CIPRO is a registered trademark of Bayer Intellectual Property GmbH, licensed to Alcon by Bayer Intellectual Property AG.
Distributed by:
Alcon Laboratories, Inc.
6201 South Freeway
Fort Worth, Texas 76134
© 2006, 2009, 2016 Novartis
T2017-38
March 2017
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0065-8531-10 | ML - Milliliter | 0065-8531 | b2462f86-5fb8-4acb-a885-401f0a630a7b | 1 | 2012-07-24 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| CIPROFLOXACIN HYDROCHLORIDE | ACTIVE INGREDIENT | 4BA73M5E37 | 6 | |
| HYDROCORTISONE | ACTIVE INGREDIENT | WI4X0X7BPJ | 6 | |
| CIPROFLOXACIN | ACTIVE MOIETY | 5E8K9I0O4U | 6 | |
| HYDROCORTISONE | ACTIVE MOIETY | WI4X0X7BPJ | 6 | |
| ACETIC ACID | INACTIVE INGREDIENT | Q40Q9N063P | 6 | |
| BENZYL ALCOHOL | INACTIVE INGREDIENT | LKG8494WBH | 6 | |
| HYDROCHLORIC ACID | INACTIVE INGREDIENT | QTT17582CB | 6 | |
| LECITHIN, SOYBEAN | INACTIVE INGREDIENT | 1DI56QDM62 | 6 | |
| POLYSORBATE 20 | INACTIVE INGREDIENT | 7T1F30V5YH | 6 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | 6 | |
| SODIUM ACETATE | INACTIVE INGREDIENT | 4550K0SC9B | 6 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | 6 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | 6 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 6 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0065-8531 | 0065-8531-10 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CIPROFLOXACIN HYDROCHLORIDE | 4BA73M5E37 | ACTIM |
| HYDROCORTISONE | WI4X0X7BPJ | ACTIB |
| POLYVINYL ALCOHOL | 532B59J990 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM ACETATE | 4550K0SC9B | IACT |
| ACETIC ACID | Q40Q9N063P | IACT |
| LECITHIN, SOYBEAN | 1DI56QDM62 | IACT |
| POLYSORBATE 20 | 7T1F30V5YH | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| HYDROCHLORIC ACID | QTT17582CB | IACT |
| BENZYL ALCOHOL | LKG8494WBH | IACT |
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, EMULSION / INTRAVENOUS | 45 mg | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | SOLUTION / INTRAVENOUS | 14 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | SPRAY, METERED / NASAL | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | SUSPENSION, EXTENDED RELEASE / INTRASYNOVIAL | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | LIQUID / INTRAVENOUS | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / ENDOTRACHEAL | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / INTRACAUDAL | ADJ PH | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | TABLET / ORAL | 231 mg | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | INJECTION / INTRALESIONAL | ADJ PH | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, SUSPENSION / INTRALESIONAL | 20 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS | 5 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | POWDER, FOR SOLUTION / ORAL | ADJ PH | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | SOLUTION / INTRA-ARTERIAL | ADJ PH | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION / INTRALESIONAL | 0.9 %w/v | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 144 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION, SOLUTION / PARENTERAL | 210 mg | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION / INTRAVENOUS | 28773 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | SOLUTION / SUBCUTANEOUS | ADJ PH | ||
| SODIUM ACETATE | SODIUM ACETATE | 4550K0SC9B | SOLUTION / TOPICAL | NA | ||
| SODIUM ACETATE | SODIUM ACETATE | 4550K0SC9B | INJECTION / SUBCUTANEOUS | 19 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, SOLUTION / INTRAVASCULAR | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / PARENTERAL | ADJ PH | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | INJECTION / INTRASYNOVIAL | ADJ PH | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | INJECTION / INTRAMUSCULAR | 1.62 %w/v | ||
| SODIUM ACETATE | SODIUM ACETATE | 4550K0SC9B | SUSPENSION/ DROPS / AURICULAR (OTIC) | 0.03 %w/v | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | SHAMPOO / TOPICAL | 8 %w/w | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | CREAM / TOPICAL | 108 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | TABLET, COATED / ORAL | NA | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / INTRA-ARTERIAL | 176 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | INJECTION / INTRALESIONAL | ADJ PH | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SUSPENSION/ DROPS / TOPICAL | 0.23 %w/v | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVERNOUS | ADJ PH | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | INJECTION / SUBCUTANEOUS | 22 mg | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | SYRUP / ORAL | 10 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | SOLUTION/ DROPS / TOPICAL | ADJ PH | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | TABLET, DELAYED RELEASE / ORAL | 2.31 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | INJECTION, SUSPENSION / INTRASYNOVIAL | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | AEROSOL, METERED / RESPIRATORY (INHALATION) | ADJ PH | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | INJECTION, SUSPENSION / INTRA-ARTICULAR | ADJ PH | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SUSPENSION / RESPIRATORY (INHALATION) | 43 mg | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | SUSPENSION / AURICULAR (OTIC) | 0.26 %w/v | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | SUSPENSION/ DROPS / AURICULAR (OTIC) | 3 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | TABLET / ORAL | 2.32 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | SUSPENSION / OPHTHALMIC | ADJ PH | ||
| ACETIC ACID | ACETIC ACID | Q40Q9N063P | INJECTION / INTRAVENOUS | 827 mg | ||
| BENZYL ALCOHOL | BENZYL ALCOHOL | LKG8494WBH | SPRAY / NASAL | 5 mg | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | SPRAY / NASAL | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, POWDER, FOR SOLUTION / RECTAL | ADJ PH | ||
| SODIUM CHLORIDE | SODIUM CHLORIDE | 451W47IQ8X | INJECTION / DENTAL | 0.4 %w/v | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | SUSPENSION / OPHTHALMIC | 0.05 %w/v | ||
| SODIUM ACETATE | SODIUM ACETATE | 4550K0SC9B | INJECTION, SUSPENSION / INTRAVITREAL | 0.39 %w/v | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS | NA | ||
| POLYSORBATE 20 | POLYSORBATE 20 | 7T1F30V5YH | SUSPENSION / AURICULAR (OTIC) | 0.1 %w/v | ||
| SODIUM ACETATE | SODIUM ACETATE | 4550K0SC9B | SUSPENSION / AURICULAR (OTIC) | 0.68 %w/v | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, SOLUTION / SUBCUTANEOUS | 1 %w/v | ||
| SODIUM ACETATE | SODIUM ACETATE | 4550K0SC9B | INJECTION / SOFT TISSUE | ADJ PH | ||
| LECITHIN, SOYBEAN | SOYBEAN LECITHIN | 1DI56QDM62 | TABLET, EXTENDED RELEASE / ORAL | 20 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | INJECTION, SOLUTION / SUBARACHNOID | ADJ PH | ||
| SODIUM HYDROXIDE | SODIUM HYDROXIDE | 55X04QC32I | TABLET, FILM COATED / ORAL | 8 mg | ||
| HYDROCHLORIC ACID | HYDROCHLORIC ACID | QTT17582CB | SOLUTION / OPHTHALMIC | 0.31 %w/v |
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| N020805-001 | CIPRO HC | CIPROFLOXACIN HYDROCHLORIDE; HYDROCORTISONE | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | AB | RLD, RS | 1998-02-10 |
| Application-product | TE code |
|---|---|
| N020805-001 | AB |
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-10-15 13:18:30 | 2026-09 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | AB | RLD, RS | 1998-02-10 | c2088c7a36db… |
| 2026-09-14 22:38:34 | 2026-08 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | AB | RLD, RS | 1998-02-10 | 84e616aacf4f… |
| 2026-08-18 06:07:40 | 2026-07 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | AB | RLD, RS | 1998-02-10 | caaa826d4ba7… |
| 2026-02-19 14:30 UTC | 2026-02 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | AB | RLD, RS | 1998-02-10 | 011fe1cb6892… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | AB | RLD, RS | 1998-02-10 | 31067a03dcf5… |
| 2025-08-23 18:47 UTC | 2025-08 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 6a471c1ec25d… | |
| 2025-03-22 03:13 UTC · 3 captures of this ZIP | 2025-03 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | fd3edfee7708… | |
| 2025-02-26 10:13 UTC · 3 captures of this ZIP | 2025-02 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | b8a1b40f171c… | |
| 2025-01-19 17:59 UTC · 7 captures of this ZIP | 2025-01 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 03ed91905a0d… | |
| 2024-12-13 21:23 UTC · 2 captures of this ZIP | 2024-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 2680178bc6a6… | |
| 2024-09-14 05:58 UTC · 2 captures of this ZIP | 2024-09 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 5bbf6a4d5a75… | |
| 2024-11-08 22:44 UTC · 3 captures of this ZIP | 2024-11 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | d8e5a09893c0… | |
| 2024-10-29 15:01 UTC | 2024-10 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | d06236e962d9… | |
| 2024-08-13 05:28 UTC · 3 captures of this ZIP | 2024-08 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 79d66fd596c7… | |
| 2024-07-13 05:37 UTC · 2 captures of this ZIP | 2024-07 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 301d65b070ca… | |
| 2024-06-18 03:08 UTC · 5 captures of this ZIP | 2024-06 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 1e350fbaab3a… | |
| 2024-05-31 18:47 UTC | 2024-05 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 8072bd15b7f6… | |
| 2022-06-29 02:47 UTC · 2 captures of this ZIP | 2022-06 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 5c6f7cd8ea54… | |
| 2022-04-08 23:34 UTC | 2022-04 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 5d02ea3f76ae… | |
| 2022-04-04 05:41 UTC | 2022-04 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 4b0b4de00fa7… | |
| 2019-12-13 00:20 UTC | 2019-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 74a2ff9319b5… | |
| 2022-03-09 01:35 UTC | 2022-03 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | bb7c543d1eb4… | |
| 2021-12-28 21:50 UTC | 2021-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 782e0a99824c… | |
| 2021-05-05 16:15 UTC · 3 captures of this ZIP | 2021-05 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 87673890dc5c… | |
| 2021-03-12 10:30 UTC | 2021-03 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 5aa47cf7b7d7… | |
| 2020-12-22 03:56 UTC | 2020-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 8869cabd3fbd… | |
| 2020-11-12 02:37 UTC | 2020-11 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | c0c555d07b60… | |
| 2019-12-14 00:12 UTC | 2019-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 3f01610625f2… | |
| 2019-09-15 20:21 UTC | 2019-09 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | b00525d2431f… | |
| 2019-07-19 19:46 UTC | 2019-07 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | ea99ee380514… | |
| 2024-03-16 18:09 UTC · 4 captures of this ZIP | 2024-03 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 6a51e52b5d6a… | |
| 2024-02-18 07:12 UTC | 2024-02 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 1c564ffb4f44… | |
| 2023-12-20 04:57 UTC | 2023-12 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | ea1830bbd6c7… | |
| 2023-11-28 05:40 UTC · 2 captures of this ZIP | 2023-11 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | a72a2bbeb626… | |
| 2023-10-25 00:34 UTC · 2 captures of this ZIP | 2023-10 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 9b2671bbb829… | |
| 2023-07-15 15:27 UTC · 2 captures of this ZIP | 2023-07 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | a67488948f0b… | |
| 2023-06-13 01:57 UTC · 3 captures of this ZIP | 2023-06 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 3f0d92c62455… | |
| 2023-05-13 08:27 UTC | 2023-05 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 053a50430f4f… | |
| 2023-01-26 05:58 UTC | 2023-01 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 3bdfa0b2c4d7… | |
| 2022-11-12 20:34 UTC · 5 captures of this ZIP | 2022-11 | N020805-001 | CIPRO HC | EQ 0.2% BASE;1% | SUSPENSION/DROPS / OTIC | RLD, RS | 1998-02-10 | 3a93d1ddd44b… |
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-10-15 13:18:30 | 2026-09 | N020805-001 | AB | 1 | c2088c7a36db… |
| 2026-09-14 22:38:34 | 2026-08 | N020805-001 | AB | 1 | 84e616aacf4f… |
| 2026-08-18 06:07:40 | 2026-07 | N020805-001 | AB | 1 | caaa826d4ba7… |
| 2026-02-19 14:30 UTC | 2026-02 | N020805-001 | AB | 1 | 011fe1cb6892… |
| 2025-12-14 10:44 UTC · 2 captures of this ZIP | 2025-12 | N020805-001 | AB | 1 | 31067a03dcf5… |
| 2026-07-26 02:55 UTC · 3 captures of this ZIP | 2026-06 | N020805-001 | AB | 1 | a50c72e98297… |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 9fccedfd-5a06-45e3-85a8-5c89687bb0e2 | 70b19501-34b6-4f95-a8dd-dd3e67d22399 | 2022-07-11 | Warnings, Adverse reactions | 9fccedfd-5a06-45e3-85a8-5c89687bb0e2 70b19501-34b6-4f95-a8dd-dd3e67d22399 |
Adverse event summaries are temporarily unavailable. Other product information remains available.