VitaPhyte Redness Reliever Lubricant Eye Drops

Manufacturer
Guangzhou Liyan Cosmetics Technology Co., Ltd.
Effective date
2026-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-12 05:10:11

Label at a glance#

ProductVitaPhyte Redness Reliever Lubricant Eye Drops
Active ingredientTETRAHYDROZOLINE, POLYETHYLENE GLYCOL 400
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Warnings

For external use only.

Ask a doctor before use if you have
• glaucoma or other serious eye conditions
• persistent eye redness or pain

When using this product
• do not touch the tip of the container to any surface
• remove contact lenses before application
• temporary blurred vision or mild stinging may occur
• overuse may increase eye redness
• discontinue use if solution changes color or becomes cloudy
• replace cap tightly after each use

Stop use and ask a doctor if
• eye pain or irritation worsens
• redness persists for more than 72 hours
• vision changes occur
• symptoms do not improve

Keep out of reach of children.
If swallowed, seek medical assistance or contact a Poison Control Center immediately.

If pregnant or breast-feeding, consult a healthcare professional before use.

INACTIVE INGREDIENT SECTION

Purified Water
Glycerin
Sodium Hyaluronate
Honey Extract(Jimerito Bee Honey)
Boric Acid
Sodium Borate
Potassium Chloride
Magnesium Chloride
Sodium Chloride
Glycine
Hydrochloric Acid and/or Sodium Hydroxide may be used to adjust pH.

INDICATIONS & USAGE SECTION

Uses

• relieves redness caused by minor eye irritation

• provides soothing moisture for dry, tired, or irritated eyes

• helps protect eyes from dryness caused by screen time, wind, dust, or sunlight

• temporarily relieves burning and discomfort associated with dry eyes

• lubricates and refreshes eyes for long-lasting comfort

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, seek medical assistance or contact a Poison Control Center immediately.

OTC - PURPOSE SECTION

Polyethylene Glycol 400 1% → Lubricant
Tetrahydrozoline HCl 0.05% → Redness reliever

DOSAGE & ADMINISTRATION SECTION

Directions

• adults and children 6 years of age and over:
instill 1 to 2 drops in the affected eye(s) as needed, up to 4 times daily

• for severe dryness or irritation:
may be used throughout the day as directed by a doctor

• remove contact lenses before use and wait at least 10 minutes before reinserting

• children under 6 years of age:
consult a doctor before use

• children under 2 years of age:
do not use

RECENT MAJOR CHANGES SECTION

Uses

• relieves redness caused by minor eye irritation

• provides soothing moisture for dry, tired, or irritated eyes

• helps protect eyes from dryness caused by screen time, wind, dust, or sunlight

• temporarily relieves burning and discomfort associated with dry eyes

• lubricates and refreshes eyes for long-lasting comfort

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87770-00187770-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VitaPhyte Redness Reliever Lubricant Eye DropsREDNESS RELIEVER LUBRICANT EYE DROPSGuangzhou Liyan Cosmetics Technology Co., Ltd.53d4e9b0-c9a0-797a-e063-6294a90ad0cf2026-06-04WarningsExact identifier
ndc (package): 87770-001-01
ndc (product): 87770-001
ndc11 (package): 87770000101
spl id: 53d4e9b0-c9a1-797a-e063-6294a90ad0cf
spl set id: 53d4e9b0-c9a0-797a-e063-6294a90ad0cf

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.