ROYCEDERM STYE RELIEF EYE SPRAY.- hypochlorous acid spray

RoyceDerm Stye Relief Eye Spray. by

Drug Labeling and Warnings

RoyceDerm Stye Relief Eye Spray. by is a Otc medication manufactured, distributed, or labeled by RoyceDerm LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Hypochlorous Acid 0.01%

PURPOSE

Antiseptic / Eyelid Cleanser

DOSAGE & ADMINISTRATION

For cleansing of the eyelid and eyelash
area

Helps reduce bacteria that can cause skin
and eyelid irritation

Supports daily eyelid hygiene

WARNINGS

For external use only

In the eyes · If the solution changes color or becomes cloudy

• Redness, irritation, or discomfort persists or worsens
• You experience allergic reaction or unexpected eye sensitivity

• Do not touch tip of container to any surface
• Avoid direct contact with the eyes
• If contact with eyes occurs, rinse thoroughly with water

• Redness, irritation,or discomfort persists or worsens
• You experience allergic reaction or unexpected eye sensitivity

If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

• Spray directly onto closed eyelids or applyusing a sterile cotton pad
• Gently wipe acrossthe eyelid and lash line
• Use 1-2 times daily oras recommended by your eye care professional
• If you wear contact lenses, please removethem before use
• For external eyelid use only

OTHER SAFETY INFORMATION

• Store at 15°-30°C(59°-86°F)
• Do not freeze
• Use within 90 days of opening
• Forsingle-patient use only

INACTIVE INGREDIENT

Electrolyzed water, Sodium chloride

QUESTIONS

• service@roycederm.com
• www.roycederm.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ROYCEDERM STYE RELIEF EYE SPRAY. 
hypochlorous acid spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85424-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.01 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85424-006-01	100 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/12/2025

Labeler - RoyceDerm LLC (130329531)