FDA.reportPublic FDA data

ANUA INVISIBLE GLOW FINISH SUNSCREEN

Manufacturer
The Founders Inc.
Effective date
2026-01-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:33:53

Label at a glance#

ProductANUA INVISIBLE GLOW FINISH SUNSCREEN
Active ingredientOCTOCRYLENE, AVOBENZONE, OCTISALATE, HOMOSALATE
Label structure2 sections

Label contents#

Full prescribing information#

Drug Facts

DESCRIPTION SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredientsActive ingredients

Purpose

OTC - PURPOSE SECTION

purpose-sunscreen stickpurpose-sunscreen stick

Other information

OTHER SAFETY INFORMATION

Other informationOther information

Directions

DOSAGE & ADMINISTRATION SECTION

DirectionsDirectionsDirections continuedDirections continued

Uses

INDICATIONS & USAGE SECTION

UsesUses

Warnings

WARNINGS SECTION

WarningsWarnings

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

  • If swallowed, get medical help or contact a Poison Control Center right away
Do not use

OTC - DO NOT USE SECTION

Do not use

  • on damaged or broken skin
Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • rash occurs
When using this product

OTC - WHEN USING SECTION

When using this product

  • Keep out of eyes. Rinse with water to remove

Inactive ingredient

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredientsInactive ingredients continuedInactive ingredients continued

Questions

OTC - QUESTIONS SECTION

QuestionsQuestions

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KDH PackageKDH Packagepackagepackage

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138800307372150GTIN-13: 8800307372150
EAN-13: 8800307372150
GTIN storage (14 digits): 08800307372150		package-sunscreen stick.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84610-300-01ANUA INVISIBLE GLOW FINISH SUNSCREEN17.5 g in 1 BOTTLESTICK17.52

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84610-30084610-300-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
SODIUM HYALURONATEYSE9PPT4THIACT
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE75D21FL1PIIACT
DIETHYLHEXYL CARBONATEYCD50O0Z6LIACT
DIBUTYL LAUROYL GLUTAMIDE3V7K3IA58XIACT
WATER059QF0KO0RIACT
DIBUTYL ETHYLHEXANOYL GLUTAMIDE0IAF2L30VSIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
DIISOSTEARYL MALATEQBS8A3XZGQIACT
DIMETHYLSILANOL HYALURONATEZ853O1D4TEIACT
HOMOSALATEV06SV4M95SACTIB
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CERAMIDE NP4370DF050BIACT
OCTYLDODECANOL461N1O614YIACT
PANTHENOLWV9CM0O67ZIACT
GLYCERINPDC6A3C0OXIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYALURONIC ACIDS270N0TRQYIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-11-07monthly-update2026-06-03 17:40:47

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
ANUA INVISIBLE GLOW FINISH SUNSCREENAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEThe Founders Inc.446ac344-1078-4cd1-e063-6294a90a4bd42026-01-19WarningsExact identifier
ndc (package): 84610-300-01
ndc (product): 84610-300
ndc11 (package): 84610030001
spl id: 48c8100d-5b29-ea3e-e063-6294a90ab076
spl set id: 446ac344-1078-4cd1-e063-6294a90a4bd4

Reported adverse events (FAERS/openFDA)#

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