SPF 20 Sunscreen UVAUVB Tinted Moisturizer Nude

Manufacturer
Hangzhou Facecare Cosmetics Co., Ltd.
Effective date
2020-12-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:34:55

Label at a glance#

ProductSPF 20 Sunscreen UVAUVB Tinted Moisturizer Nude
Active ingredientOCTISALATE, OCTINOXATE, OXYBENZONE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Octinoxate: 7.5%

Octisalate: 5%

Oxybenzone: 3%

OTC - PURPOSE SECTION

Purpose:

Sunscreen

INDICATIONS & USAGE SECTION

Uses:

Helps prevent sunburn

WARNINGS SECTION

Warning:

For external use only

Skin Cancer/ Skin Aging Alert: Spending time in the sun increases your risk of skin cancer or early skin aging. This product has been shown to only protect you from sunburn, not skin cancer or sking aging.

Do not use on damage or broken skin

OTC - WHEN USING SECTION

When using this product:

Keep out of eyes. Rinse with water to remove.

OTC - ASK DOCTOR SECTION

Stop Use and Ask a Doctor if r ash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

DOSAGE & ADMINISTRATION SECTION

Directions:

For sunscreen use:

Apply generously 15 min before sun exposure.

Apply to clean skin in an upward and outward motion with sponage or foundation brush

Children under six months of age: ask a doctor.

Reapply at least every two hours.

Use a water resistant sunscreen if swimming or sweating

Sun Protection Measures:

Spending time in sun increases your risk of skin cancer or early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF value of 15 or higher and other sun protection measures including

  • Limit time in the sun, especially from 10 am to 2 pm
  • Wear long sleeved shirts, pants, hats, and sunglasses.
  • Children under six months of age: ask a doctor

Other Information:

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

Store at room temperature 15-30 C (59-86F)

INACTIVE INGREDIENT SECTION

Inactive Ingredient:

Water, Dimethicone, Propylene Glycol,  C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Steareth-21, Steareth-2, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Phenoxyethanol, Caprylyl Glycol, Ethylhexyglycerin, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Xantahn Gum, Retinyl Palmitate (VA), Ascorbyl Palmitate (VC), Tocopheryl Acetate (VE), Butylene Glycol, Aloe Barbadensis Leaf Extract, Cucumis Sativus (Cucumber) Fruit Extract

May contain:

Titanium Oxide, Iron Oxides (CI 77491, CI 77492, CI 77499)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52664-633-012022-01-28C16284748780-1d6a99b39-66ea-a426-e053-dadaa90af4c2Drug Fact

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52664-633-01SPF 20 Sunscreen UVAUVB Tinted Moisturizer Nude25 mL in 1 BOTTLECREAM252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52664-633SPF 20 SUNSCREEN UVAUVB TINTED MOISTURIZER NUDE (OCTISALATE) CREAM [HANGZHOU FACECARE COSMETICS CO., LTD.]2Legacy NDC, 1 package rows20201211_97b96a11-86ad-339e-e053-2995a90a88d3.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52664-63352664-633-01

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
b61febf7-287f-8df2-e053-2a95a90a3f2e97b96a11-86ad-339e-e053-2995a90a88d32020-12-10WarningsExact identifier
spl id: b61febf7-287f-8df2-e053-2a95a90a3f2e
spl set id: 97b96a11-86ad-339e-e053-2995a90a88d3

Reported adverse events (FAERS/openFDA)#

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