Revlon Nearly Naked Makeup

Manufacturer
Revlon Consumer Products Corp | REVLON, INC.
Effective date
2016-11-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:04

Label at a glance#

ProductRevlon Nearly Naked Makeup
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure8 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

•Apply liberally 15 minutes before sun exposure •Use a water resistant sunscreen if swimming or sweating •Reapply at least every 2 hours •Children under 6 months: Ask a doctor.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Octinoxate: 3.5%

Titanium Dioxide 9.5%

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 notuse on damaged or broken skin
•When using this product: Keep out of eyes. Rinse with water to remove.
•Stop use and ask a doctor if a rash occurs
•Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control center right away

Directions

INSTRUCTIONS FOR USE SECTION

•Apply liberally 15 minutes before sun exposure
•Use a water resistant sunscreen if swimming or sweating
•Reapply at least every 2 hours
•Children under 6 months: Ask a doctor.

Sun Protection Measures

OTC - WHEN USING SECTION

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 am - 2 pm
•Wear long-sleeved shirts, pants, hats and sunglasses.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

AQUA ((WATER) EAU), CYCLOPENTASILOXANE, DIMETHICONE, GLYCERIN, PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIMETHYLSILOXYSILICATE, PHENYL TRIMETHICONE, BORON NITRIDE, DISTEARDIMONIUM HECTORITE, DIMETHICONE/PEG-10/15 CROSSPOLYMER, ALUMINA, SILICA, CAPRYLYL GLYCOL, PHENOXYETHANOL, LAURETH-7, SODIUM CHLORIDE, DIMETHICONE CROSSPOLYMER, METHICONE, XANTHAN GUM, POTASSIUM SORBATE, TRIETHOXYCAPRYLYLSILANE, SODIUM ASCORBYL PHOSPHATE, NIACINAMIDE, HYDROLYZED OAT FLOUR, TETRASODIUM EDTA, TOCOPHERYL ACETATE, C12-15 ALKYL BENZOATE, TOCOPHEROL, SODIUM CITRATE, DIPROPYLENE GLYCOL, SODIUM LAUROYL LACTYLATE, CAMELLIA SINENSIS LEAF EXTRACT, LINOLEIC ACID, LECITHIN, METHOXY AMODIMETHICONE/SILSESQUIOXANE COPOLYMER, PHYTOSTERYL CANOLA GLYCERIDES, PALMITIC ACID, OLEIC ACID, CERAMIDE 3, STEARIC ACID, TRIOLEIN, HYDROGENATED JOJOBA OIL, PHYTOSPHINGOSINE, CERAMIDE 6 II, CHOLESTEROL, CARBOMER, CERAMIDE 1

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REVLON

Nearly Naked Makeup

Broad Spectrum

SPF 20

1.0 fL. OZ/30 mL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10967-622-012020-01-31C16284748780-19d75b9d0-e557-f424-e053-dadaa90a57ceRevlon Nearly Naked Makeup

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10967-622-01Revlon Nearly Naked Makeup30 mL in 1 BOTTLE, GLASSLIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10967-622REVLON NEARLY NAKED MAKEUP (OCTINOXATE, TITANIUM DIOXIDE MAKE-UP) LIQUID [REVLON CONSUMER PRODUCTS CORP]1Legacy NDC, 1 package rows20161129_a8e84e40-1c8c-41c8-9d3c-d632e7715564.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 44 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-62210967-622-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 42 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
42748194-73f1-5470-e054-00144ff8d46ca8e84e40-1c8c-41c8-9d3c-d632e77155642016-11-29WarningsExact identifier
spl id: 42748194-73f1-5470-e054-00144ff8d46c
spl set id: a8e84e40-1c8c-41c8-9d3c-d632e7715564

Reported adverse events (FAERS/openFDA)#

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