Drug Facts

Manufacturer
L’Oreal USA Products Inc | L’Oreal USA, Inc.
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:19:09

Label at a glance#

ProductVichy Laboratoires Ideal Capital Soleil 60 Sunscreen Broad Spectrum SPF 60 Water Resistant 40 Minutes
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE
Label structure13 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

For sunscreen use: ●  apply liberally 15 minutes before sun exposure ●  reapply:     ●  after 40 minutes of swimming or sweating     ●  immediately after towel drying     ●  at least every 2 hours ● Sun Protection Measures . 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 value of 15 or higher and other su...

Storage and handling

protect the product in this container from excessive heat and direct sun

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 5%

Oxybenzone 6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

●  apply liberally 15 minutes before sun exposure

●  reapply:

    ●  after 40 minutes of swimming or sweating

    ●  immediately after towel drying

    ●  at least every 2 hours

● Sun Protection Measures. 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 value of 15 or higher and other sun protection measures including:

     ● limit time in the sun, especially from 10 a.m. – 2 p.m.

     ● wear long-sleeved shirts, pants, hats, and sunglasses

●  children under 6 months of age: Ask a doctor

Other information

STORAGE AND HANDLING SECTION

protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, silica, styrene/acrylates copolymer, butyloctyl salicylate, glycerin, poly C10-30 alkyl acrylate, PEG-100, stearate, glyceryl stearate, caprylyl methicone, trisiloxane, dicaprylyl carbonate, phenoxyethanol, potassium cetyl phosphate, dimethicone, caprylyl glycol, cyclopentasiloxane, PEG-8 laurate, methylparaben, inulin lauryl carbamate, chlorphenesin, triethanolamine, ethylparaben, acrylates/C10-30 alkyl acrylate crosspolymer, xanthan gum, disodium EDTA, dimethicone crosspolymer, tocopherol, vitis vinifera (grape) fruit extract, citric acid, sodium benzoate, potassium sorbate

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-877-378-4249

Monday - Friday (9 a.m. to 5 p.m. EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-88949967-889-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
3a882254-ab2c-42c5-986e-3c85e45247240d768286-1ec9-4396-8b1a-e0a4c4b4dac32023-01-26WarningsExact identifier
spl set id: 0d768286-1ec9-4396-8b1a-e0a4c4b4dac3

Reported adverse events (FAERS/openFDA)#

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