Visage Pro Peach Fuzz

Manufacturer
CA-Botana International
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
monthly-update
Hydrated at
2026-06-03 17:46:15

Label at a glance#

ProductVisage Pro Peach Fuzz
Active ingredientOCTISALATE, OCTOCRYLENE, AVOBENZONE, OCTINOXATE, HOMOSALATE
Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.5%............................................. Sunscreen

Homosalate 7%............................................Sunscreen

Octisalate 5%..............................................Sunscreen

Octocrylene 7%...............................................Sunscreen

Octinoxate 2.5%.............................................Sunscreen

Purpose

OTC - PURPOSE SECTION

Sunscreen

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Inactive Ingredients

INACTIVE INGREDIENT SECTION

.

Acrylates/C10-30 Alkyl Acrylate CrosspolymerC12-15 Alkyl Benzoate, Cetearyl Alcohol, Cetearyl Olivate, Coco-Caprylate/Caprate

Decyl Oleate, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Niacinamide, Phenoxyethanol, Potassium Sorbate,

Sodium Phytate, Sorbitan Olivate, Tocopheryl Acetate, Triethanolamine, Water/Aqua, Xanthan Gum

Safety information

OTHER SAFETY INFORMATION

Protect this product from excessive heat and direct sun

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Helps prevent sunburn. If used as directed with other sun protection measured decreases the risk of skin cancer and early skin aging caused by the sun. Apply liberally 15 minutes before sun exposure. Usea water resistant sunscreen if swimming or sweating. Reapply : at least 2 hours. Children under 6 months: Ask a doctor. Sun protections measurements. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and othe sun protection measures including: limit time in the sun, specially from 10 a.m.- 2 p.m Wear long-sleeveshirts, pants, hats, and sunglasses. Protect this product from excessive heat and direct sun.

Warnings

WARNINGS SECTION

For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. If product is swallowed get medical help or contact a poison Control Center right away.

Indications & Usage

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before exposure, use water resistant sunscreen, if swimming or sweating. reapply at least every 2 hours. Children under 6 months: ask a doctor

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Screen shotScreen shot

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35192-04735192-047-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 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
4b344f6e-f9ca-d197-e063-6394a90a67e7e64e1469-47ee-f069-e053-2a95a90a8aa32026-02-19WarningsExact identifier
spl set id: e64e1469-47ee-f069-e053-2a95a90a8aa3

Reported adverse events (FAERS/openFDA)#

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