Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED PRED MILD ® (prednisolone acetate ophthalmic suspension, USP) 0.12% is supplied sterile in opaque white LDPE plastic bottles with droppers with pink high impact polystyrene (HIPS) caps as follows: 5 mL in 10 mL bottle - NDC 11980-174-05 10 mL in 15 mL bottle - NDC 11980-174-10 Storage : Store at 15°C to 25°C (59°F to 77°F) in an upright position. Protect from freezing. Revised : 11/2025 Distributed by: AbbVie, Inc. North Chicago, IL 60064 © 2025 AbbVie. All rights reserved. Pred Mild and its design are trademarks of Allergan, Inc., an AbbVie company. 20095922 Shape Description automatically generated; PRINCIPAL DISPLAY PANEL NDC 11980-174-10 Rx Only PRED MILD ® (prednisolone acetate ophthalmic suspension, USP) 0.12% FOR TOPICAL OPHTHALMIC USE sterile 10 mL PRINCIPAL DISPLAY PANEL NDC 11980-174-10 Rx Only PRED MILD® (prednisolone acetate ophthalmic suspension, USP) 0.12% FOR TOPICAL OPHTHALMIC USE sterile 10 mL
- HOW SUPPLIED PRED MILD ® (prednisolone acetate ophthalmic suspension, USP) 0.12% is supplied sterile in opaque white LDPE plastic bottles with droppers with pink high impact polystyrene (HIPS) caps as follows: 5 mL in 10 mL bottle - NDC 11980-174-05 10 mL in 15 mL bottle - NDC 11980-174-10 Storage : Store at 15°C to 25°C (59°F to 77°F) in an upright position. Protect from freezing. Revised : 11/2025 Distributed by: AbbVie, Inc. North Chicago, IL 60064 © 2025 AbbVie. All rights reserved. Pred Mild and its design are trademarks of Allergan, Inc., an AbbVie company. 20095922 Shape Description automatically generated
- PRINCIPAL DISPLAY PANEL NDC 11980-174-10 Rx Only PRED MILD ® (prednisolone acetate ophthalmic suspension, USP) 0.12% FOR TOPICAL OPHTHALMIC USE sterile 10 mL PRINCIPAL DISPLAY PANEL NDC 11980-174-10 Rx Only PRED MILD® (prednisolone acetate ophthalmic suspension, USP) 0.12% FOR TOPICAL OPHTHALMIC USE sterile 10 mL
Overview
PRED MILD ® (prednisolone acetate ophthalmic suspension, USP) 0.12% is a sterile, topical anti-inflammatory agent for ophthalmic use. Its chemical name is 11ß,17, 21-Trihydroxypregna-1,4-diene-3, 20-dione 21-acetate and it has the following structure: Structural Formula: prednisolone acetate Active: prednisolone acetate (microfine suspension) 0.12%. Inactives: benzalkonium chloride as preservative; boric acid; edetate disodium; hypromellose; polysorbate 80; purified water; sodium bisulfite; sodium chloride; and sodium citrate. The pH during its shelf life ranges from 5.0 - 6.0. The following structure for PRED MILD® (prednisolone acetate ophthalmic suspension, USP) 0.12% is a sterile, topical anti-inflammatory agent for ophthalmic use. Its chemical name is 11ß,17, 21-Trihydroxypregna-1,4-diene-3, 20-dione 21-acetate.
Indications & Usage
PRED MILD ® is indicated for the treatment of mild to moderate noninfectious allergic and inflammatory disorders of the lid, conjunctiva, cornea, and sclera (including chemical and thermal burns).
Dosage & Administration
Shake well before using. Instill one to two drops into the conjunctival sac two to four times daily. During the initial 24 to 48 hours, the dosing frequency may be increased if necessary. Care should be taken not to discontinue therapy prematurely. If signs and symptoms fail to improve after 2 days, the patient should be re-evaluated (see PRECAUTIONS ).
Warnings & Precautions
WARNINGS Prolonged use of corticosteroids may result in posterior subcapsular cataract formation and may increase intraocular pressure in susceptible individuals, resulting in glaucoma with damage to the optic nerve, defects in visual acuity and fields of vision. Prolonged use may also suppress the host immune response and thus increase the hazard of secondary ocular infections. If this product is used for 10 days or longer, intraocular pressure should be routinely monitored even though it may be difficult in children and uncooperative patients. Steroids should be used with caution in the presence of glaucoma. Intraocular pressure should be checked frequently. Various ocular diseases and long-term use of topical corticosteroids have been known to cause corneal and scleral thinning. Use of topical corticosteroids in the presence of thin corneal or scleral tissue may lead to perforation. Acute purulent infections of the eye may be masked or activity enhanced by the presence of corticosteroid medication. The use of steroids after cataract surgery may delay healing and increase the incidence of bleb formation. Use of ocular steroids may prolong the course and may exacerbate the severity of many viral infections of the eye (including herpes simplex). Employment of a corticosteroid medication in the treatment of patients with a history of herpes simplex requires great caution; frequent slit lamp microscopy is recommended. PRED MILD ® suspension contains sodium bisulfite, a sulfite that may cause allergic-type reactions, including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in non-asthmatic people.
Contraindications
PRED MILD ® suspension is contraindicated in acute untreated purulent ocular infections, in most viral diseases of the cornea and conjunctiva including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. PRED MILD ® suspension is also contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids.
Adverse Reactions
The following adverse reactions have been identified during use of PRED MILD ® . Because reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. Adverse reactions include elevation of intraocular pressure (IOP) with possible development of glaucoma and infrequent optic nerve damage, posterior subcapsular cataract formation, and delayed wound healing. The development of secondary ocular infection (bacterial, fungal, and viral) has occurred. Fungal and viral infections of the cornea are particularly prone to develop coincidentally with long-term applications of steroids. The possibility of fungal invasion should be considered in any persistent corneal ulceration where steroid treatment has been used (see PRECAUTIONS ). Other adverse reactions reported with the use of prednisolone acetate ophthalmic suspension include: allergic reactions; dysgeusia; eye pain; foreign body sensation; headache; pruritus; rash; transient burning and stinging upon instillation and other minor symptoms of ocular irritation; urticaria; and visual disturbance (blurry vision). Keratitis, conjunctivitis, corneal ulcers, mydriasis, conjunctival hyperemia, loss of accommodation and ptosis have occasionally been reported following local use of corticosteroids. Corticosteroid-containing preparations have also been reported to cause acute anterior uveitis and perforation of the globe.
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