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Drug Facts
Moisture Oyster Solution/ Drops
FDA Label NDC 87105-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Moisture Oyster Inc for the product Moisture Oyster (NDC 87105-100). 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 other, active ingredient, purpose, uses, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Glycerin 0.25%
Purpose
Eye lubricant
Uses
For the temporary relief of burning and irritation due to dryness of the eye
For the temporary relief of discom- fort due to minor irritations of the eye or to exposure to wind or sun
For use as a protectant against further irritation or to relieve dryness of the eye.
Warnings
- For external use only
Otc - Do Not Use
- Do not use ifsolution changes color or becomes cloudy.
- If tamper evident ring is broken or missing.
Otc - When Using
- To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
Otc - Stop 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.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Instill 1 or 2 drops in the affected eye(s) as needed.
Other Information
- Store at 59°-86°F (15°-30°C).
Inactive Ingredients
Borate, boric acid, calcium chloride, l-carnitine, sodium chloride, sodium hyaluronate
Principal Display Panel - 10 Ml Bottle Carton
Carton (085 Label 10ml Fda Template 20250304 M1)
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