RIPPLE- glycerin, povidone solution/ drops

Ripple by

Drug Labeling and Warnings

Ripple by is a Otc medication manufactured, distributed, or labeled by CorneaCare Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center
(1-800-222-1222)right away. ►

PURPOSE

Eye Lubricant

WARNINGS

Warnings
For external use only
Do not use
■If solution changes color or becomes cloudy.
■lf you are sensitive to any ingredient in this product.
When using this product
■Do not touch tip of container to any surface to
avoid contamination.
■Replace cap after using.
Stop use and ask a doctor if
■You experience eye pain, changes in vision,
continued redness or irritation of the eye.
■ Condition worsens or persists for more than 72 hours.

INDICATIONS & USAGE

Uses

For temporary relief of burning and irritation due to dryness of the eye.

For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun

For use as a protectant against irritation or to relieve dryness of the eye.

DOSAGE & ADMINISTRATION

Instill 1 or 2 drops in the eye(s) as needed.

ACTIVE INGREDIENT

Glycerin 0.63%
Povidone 0.25%

INACTIVE INGREDIENT

Inactive ingredients
boric acid, calcium chloride, magnesium chloride, potassium chloride ,purified water, sodium borate, sodium chloride, sodium hyaluronate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RIPPLE 
glycerin, povidone solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82875-003
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.63 g  in 100 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E)	POVIDONE	0.25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SODIUM BORATE (UNII: 91MBZ8H3QO)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BORIC ACID (UNII: R57ZHV85D4)
WATER (UNII: 059QF0KO0R)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82875-003-10	1 in 1 BOX	08/02/2025
1		10 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	08/02/2025

Labeler - CorneaCare Inc (117781728)