FDA.reportPublic FDA data

Duke Cannon Standard Issue Face

Manufacturer
RNA PHARMA, LLC
Effective date
2021-09-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:29

Label at a glance#

ProductDuke Cannon Standard Issue Face
Active ingredientOCTISALATE, AVOBENZONE, HOMOSALATE, OXYBENZONE, OCTINOXATE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredientsactive ingredients

OTC - PURPOSE SECTION

purposepurpose

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label principalpackage label principal

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60717-906-172025-01-30C16284748780-12cef2736-af0a-d83d-e063-dadaa90ab31fcc86eead-7c6c-71e1-e053-2995a90ad1ef

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-906-17Duke Cannon Standard Issue Face50 mL in 1 TUBELOTION501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60717-906DUKE CANNON STANDARD ISSUE FACE (SUNSCREEN) LOTION [RNA PHARMA, LLC]1Legacy NDC, 1 package rows20210923_cc86eead-7c6c-71e1-e053-2995a90ad1ef.zip

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-90660717-906-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
XANTHAN GUMTTV12P4NEEIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETEARYL OLIVATE58B69Q84JOIACT
OCTISALATE4X49Y0596WACTIB
EDETATE DISODIUM7FLD91C86KIACT
ETHYLHEXYL PALMITATE2865993309IACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)Q7UI015FF9IACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OXYBENZONE95OOS7VE0YACTIB
OCTINOXATE4Y5P7MUD51ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
RICE BRANR60QEP13ICIACT
ROSEMARYIJ67X351P9IACT
TOCOPHEROLR0ZB2556P8IACT
CAPRYLYL GLYCOL00YIU5438UIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
GLYCERYL 1-STEARATE258491E1RZIACT
MENTHYL LACTATE, (-)-2BF9E65L7IIACT
SORBITAN OLIVATEMDL271E3GRIACT
EICOSYL POVIDONEXQQ9MKE2BJIACT
SILICON DIOXIDEETJ7Z6XBU4IACT

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
cc86eead-7c6d-71e1-e053-2995a90ad1efcc86eead-7c6c-71e1-e053-2995a90ad1ef2021-09-21Exact identifier
spl id: cc86eead-7c6d-71e1-e053-2995a90ad1ef
spl set id: cc86eead-7c6c-71e1-e053-2995a90ad1ef

Reported adverse events (FAERS/openFDA)#

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