NIVEA MEN Age Defense Face Moisturizer

Manufacturer
Beiersdorf Inc
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:30:00

Label at a glance#

ProductNIVEA MEN Age Defense Face Moisturizer
Active ingredientHOMOSALATE, OCTOCRYLENE, AVOBENZONE, OCTISALATE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 10%

OTC - PURPOSE SECTION

Purpose

Sunscreens

INDICATIONS & USAGE SECTION

Uses

•
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 SECTION

Warnings

For external use only

.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs

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.

DOSAGE & ADMINISTRATION SECTION

Directions

For sunscreen use:

• apply liberally 15 minutes before sun exposure

• use a water resistant sunscreen if swimming or sweating

• reapply 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.

• children under 6 months of age: Ask a doctor.

OTHER SAFETY INFORMATION

Other information

protect this product from excessive heat and direct sun

INACTIVE INGREDIENT SECTION

Inactive ingredients


Water, Glycerin, Alcohol Denat., Ethylhexyl Cocoate, Isopropyl Palmitate, Isoamyl Laurate, Cetearyl Alcohol, Cocoglycerides, Tapioca Starch, Oryza Sativa (Rice) Starch, Sodium Hyaluronate, Tocopheryl Acetate, Retinyl Palmitate, Tocopherol, Behenyl Alcohol, Silica Dimethyl Silylate, Methylpropanediol, Dehydroxanthan Gum, Trisodium Ethylenediamine Disuccinate, Sodium Stearoyl Glutamate, Caprylyl Glycol, Fragrance, Phenoxyethanol, Ethylhexylglycerin, Sodium Chloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NIVEA MEN

Age Defense Daily Face Moisturizer

30

Broad spectrum SPF 30

Sunscreen Lotion

Hyaluronic acid

Pro-Retinol

24 hour moisture*

Helps protect skin from aging caused by the sun

*for sun protection use as directed

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10356-580-05NIVEA MEN Age Defense Face Moisturizer50 g in 1 BOTTLE, PUMPLOTION502
10356-580-05NIVEA MEN Age Defense Face Moisturizer1 in 1 CARTONLOTION12

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10356-58010356-580-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
NIVEA MEN Age Defense Face MoisturizerAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEBeiersdorf Inc27cbec3e-e811-6498-e063-6394a90ada492025-12-31WarningsExact identifier
ndc (package): 10356-580-05
ndc (product): 10356-580
ndc11 (package): 10356058005
spl id: 474abcc4-f19c-78f2-e063-6294a90a3f7d
spl set id: 27cbec3e-e811-6498-e063-6394a90ada49

Reported adverse events (FAERS/openFDA)#

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