SPF 15 SELFIE BOV Continuous Spray

Manufacturer
OL Products, Inc.
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:36:16

Label at a glance#

ProductSunscreen
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTISALATE
Label structure9 sections

Label contents#

Full prescribing information#

Drug Facts Acitve Ingredients Purpose

OTC - ACTIVE INGREDIENT SECTION

Drug Facts Active Ingredients PurposeDrug Facts Active Ingredients Purpose

Directions

DOSAGE & ADMINISTRATION SECTION

DirectionDirection

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

WarningsWarnings

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive Ingredients

Uses

INDICATIONS & USAGE SECTION

UsesUses

Questions

OTC - QUESTIONS SECTION

QuestionsQuestions

Selfie SPF 15 - Flammable

WARNINGS SECTION

FlammableFlammable

STORAGE AND HANDLING SECTION

Keep Out of Heat and Direct SunKeep Out of Heat and Direct Sun

SPF 15 Continuous Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF 15 Continuous SpraySPF 15 Continuous Spray

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72239-001-012022-01-28C16284748780-1d6a99b39-cecc-a426-e053-dadaa90af4c2SPF 15 SELFIE BOV Continuous Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72239-001-01Sunscreen241 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY2414

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72239-001SUNSCREEN (OCTOCRYLENE, OCTISALATE, AVOBENZONE) AEROSOL, SPRAY [OL PRODUCTS, INC.]4Legacy NDC, 1 package rows20210101_676335de-4a14-f8d7-e053-2a91aa0ab97c.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72239-00172239-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
WATER059QF0KO0RIACT

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
b7ceac19-93b5-1ea6-e053-2995a90a14e5676335de-4a14-f8d7-e053-2a91aa0ab97c2020-12-31WarningsExact identifier
spl id: b7ceac19-93b5-1ea6-e053-2995a90a14e5
spl set id: 676335de-4a14-f8d7-e053-2a91aa0ab97c

Reported adverse events (FAERS/openFDA)#

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