FDA.reportPublic FDA data

Sensitive Skin 8 oz

Manufacturer
Walgreen Company
Effective date
2018-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:57:16

Label at a glance#

ProductSensitive Skin 8 oz
Active ingredientOCTOCRYLENE, ZINC OXIDE
Label structure10 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 reapply: • after 80 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 of 15 or higher and other sun protection measures including: • limit time in t...

Storage and handling

Protect the product in this container from excessive heat and direct sun Store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Walgreens Sensitive Skin Sunscreen Lotion

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octocrylene 4.0%, Zinc Oxide 5.0%  

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

OTC - STOP USE SECTION

if 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.

May stain some fabrics

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • reapply:
    • after 80 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 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-sleeve shirts, pants, hats, and sunglasses
  • children under 6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Ethylhexyl Stearate, Disopropyl Adipate, Cetyl Dimethicone, Polyglycery-4 Isosteate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Isohexadecane, Beeswax, Aloe Barbadensis Leaf Juice, Dimethicone, Hydrogenated Castor Oil, Silica, Triethoxycaprylylsilane, Caprylyl Glycol, Tocopherol Acetate, Phenoxyethanol, Disodium EDTA, Sodium Chloride

Other Information

STORAGE AND HANDLING SECTION

  • Protect the product in this container from excessive heat and direct sun
  • Store at room temperature

Questions or comments?

OTC - QUESTIONS SECTION

www.walgreens.com or call toll free 1-800-925-4733

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50
Sensitive Skin
Broad spectrum SPF 50
Sunscreen UVA/UVB
Oxybenzone Free

Fragrance Free

Oil Free

Dermatologist test

Water Resistant (80 minutes)
8 FL OZ (236.5 mL)

PRINCIPAL DISPLAY PANEL 50 Sensitive Skin Broad spectrum SPF 50 Sunscreen UVA/UVB Oxybenzone Free Fragrance Free Oil Free Dermatologist test Water Resistant (80 minutes) 8 FL OZ...PRINCIPAL DISPLAY PANEL 50 Sensitive Skin Broad spectrum SPF 50 Sunscreen UVA/UVB Oxybenzone Free Fragrance Free Oil Free Dermatologist test Water Resistant (80 minutes) 8 FL OZ...

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-8224-842020-09-27C16284748780-1ab0e2407-27d3-f274-e053-dbdaa90a6471Sensitive Skin 8 oz
0363-8224-842020-09-25C16284748780-1ab0e2407-27d3-f274-e053-dbdaa90a6471Sensitive Skin 8 oz
0363-8224-842020-07-22C16284748780-1ab0e2407-27d3-f274-e053-dbdaa90a6471Sensitive Skin 8 oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-8224-84Sensitive Skin 8 oz236.5 mL in 1 BOTTLELOTION236.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-8224SENSITIVE SKIN 8 OZ (OCTOCRYLENE, ZINC OXIDE) LOTION [WALGREEN COMPANY]1Legacy NDC, 1 package rows20181115_468c0c86-7ec5-4d5c-b413-98df1dbe8d6f.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-82240363-8224-84

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
HEXYL LAURATE4CG9F9W01QIACT
ISOHEXADECANE918X1OUF1EIACT
YELLOW WAX2ZA36H0S2VIACT
ALOE VERA LEAFZY81Z83H0XIACT
DIMETHICONE92RU3N3Y1OIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SODIUM CHLORIDE451W47IQ8XIACT

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
b2994a9b-c839-4fe1-8821-7cbf1faae327468c0c86-7ec5-4d5c-b413-98df1dbe8d6f2018-09-17WarningsExact identifier
spl id: b2994a9b-c839-4fe1-8821-7cbf1faae327
spl set id: 468c0c86-7ec5-4d5c-b413-98df1dbe8d6f

Reported adverse events (FAERS/openFDA)#

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