Active Ingredients
Mineral oil (20%)
White petrolatum (80%)
Retaine Pm Ointment
FDA Label NDC 54799-893
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ocusoft Llc for the product Retaine Pm (NDC 54799-893). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Eye lubricant
Uses
As a lubricant to prevent further irritaion or to relieve dryness of the eye(s).
Warnings
For use in the eyes only.
When Using This Product
● do not touch tip of container to any surface to avoid contamination.
● replace cap after use.
Stop Use And Ask A Doctor If
● you experience eye pain, changes in vision, continued redness or irritation of the eye.
● the condition worsens or persists for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
● Pull down the lower lid of the affected eye(s).
● Apply a small amount (1/4 inch) of ointment to the inside of the eyelid.
Other Information
● Do not use if cap breakaway seal is broken or missing.
● Store between 15°-30°C (59°-86°F).
● Keep this carton for full product information.
Questions?
☎ Call
(800) 233-5469 M-F
8:30AM-5:00PM CST
or visit retainebrand.com
Package Label. Principal Display Panel
Retaine Pm (F1)
Retaine Pm (F2)
Retaine Pm (Bs)
Retaine Pm (3 5)
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