Sunscreen

Manufacturer
O.L. Products, Inc, | O.L. Products, Inc.
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:36:17

Label at a glance#

ProductSunscreen
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure10 sections

Label contents#

Full prescribing information#

Drug Facts Active Ingredients Purpose

OTC - ACTIVE INGREDIENT SECTION

ActivesActives

Uses

INDICATIONS & USAGE SECTION

UsesUses

Directions

DOSAGE & ADMINISTRATION SECTION

InstructionsInstructions

Inactive ingredients

INACTIVE INGREDIENT SECTION

InactivesInactives

Other information

GENERAL PRECAUTIONS SECTION

General PrecautionsGeneral Precautions

Questions or Comments?

OTC - QUESTIONS SECTION

QuestionsQuestions

Warnings For external use only When using this product Stop use and ask a doctor Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings and PrecautionsWarnings and Precautions

OTC - PURPOSE SECTION

PurposePurpose

WARNINGS SECTION

WarningsWarnings

SPF 30 Spay Gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front PanelFront Panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72239-002-012022-01-28C16284748780-19d75b9d0-36d6-f424-e053-dadaa90a57ceSPF 30 SELFIE
72239-002-012020-07-27C16284748780-19d75b9d0-36d6-f424-e053-dadaa90a57ceSPF 30 SELFIE
72239-002-012020-01-31C16284748780-19d75b9d0-36d6-f424-e053-dadaa90a57ceSPF 30 SELFIE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72239-002-01Sunscreen234 g in 1 BOTTLE, SPRAYSPRAY2343

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72239-002SUNSCREEN (SELFIE SPF30 SPRAY LOTION) SPRAY [O.L. PRODUCTS, INC,]3Legacy NDC, 1 package rows20210101_6a1f637d-3b3d-9714-e053-2a91aa0a5abc.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72239-00272239-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b7ced1e8-2607-e9fa-e053-2995a90a66376a1f637d-3b3d-9714-e053-2a91aa0a5abc2020-12-31WarningsExact identifier
spl id: b7ced1e8-2607-e9fa-e053-2995a90a6637
spl set id: 6a1f637d-3b3d-9714-e053-2a91aa0a5abc

Reported adverse events (FAERS/openFDA)#

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