ANUA ZERO-CAST MOISTURIZING FINISH SUNSCREEN

Manufacturer
The Founders Inc. | ENGLEWOOD LAB, INC.
Effective date
2026-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:33:50

Label at a glance#

ProductANUA ZERO-CAST MOISTURIZING FINISH SUNSCREEN
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure2 sections

Label contents#

Full prescribing information#

Drug Facts

DESCRIPTION SECTION

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 7.0%

Octisalate 5.0%

Octocrylene 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 if

OTC - STOP USE SECTION

■ 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.

Directions

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:

■ Apply liberally 15 minutes before sun exposure

■ Reapply:

■ after 80 minutes of swimming or sweating

■ immediately after towel drying

■ at least every 2 hours

■ Children under 6 months of age: Ask a doctor

■ 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 value 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-sleeved shirts, pants, hats, and sunglasses

Other information

OTHER SAFETY INFORMATION

■ Protect the product in this container from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Butyloctyl Salicylate, Glycerin, Dimethicone, Poly C10-30 Alkyl Acrylate, VP/Eicosene Copolymer, Cetearyl Alcohol, Niacinamide, Sodium Stearoyl Glutamate, Ammonium Polyacryloyldimethyl Taurate, Hydroxyacetophenone, Phenoxyethanol, Tocopheryl Acetate, Panthenol, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Xanthan Gum, 1,2-Hexanediol, Sodium Hyaluronate

Questions?

OTC - QUESTIONS SECTION

+1-888-899-9083

Monday–Friday (9 a.m.–5 p.m. EST)

www.anua.us

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

KDH PackageKDH Package

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84610-200-01ANUA ZERO-CAST MOISTURIZING FINISH SUNSCREEN50 mL in 1 TUBECREAM503
84610-200-01ANUA ZERO-CAST MOISTURIZING FINISH SUNSCREEN1 in 1 CARTONCREAM13

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84610-20084610-200-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
ANUA ZERO-CAST MOISTURIZING FINISH SUNSCREENAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEThe Founders Inc.31af7b5e-2bd6-63ee-e063-6294a90a08062026-01-19WarningsExact identifier
ndc (package): 84610-200-01
ndc (product): 84610-200
ndc11 (package): 84610020001
spl id: 48c8100d-5b2a-ea3e-e063-6294a90ab076
spl set id: 31af7b5e-2bd6-63ee-e063-6294a90a0806

Reported adverse events (FAERS/openFDA)#

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