NIVEA MEN AGE DEFENSE FACE MOISTURIZER- avobenzone, homosalate, octisalate, octocrylene lotion

NIVEA MEN Age Defense Face Moisturizer by

Drug Labeling and Warnings

NIVEA MEN Age Defense Face Moisturizer by is a Otc medication manufactured, distributed, or labeled by Beiersdorf Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 10%

PURPOSE

Purpose

Sunscreens

INDICATIONS & USAGE

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

Warnings

For external use only

.

DO NOT USE

Do not use on damaged or broken skin.

WHEN USING

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

STOP USE

Stop use and ask a doctor if rash occurs

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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

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

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

INGREDIENTS AND APPEARANCE

NIVEA MEN AGE DEFENSE FACE MOISTURIZER 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10356-580
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TAPIOCA STARCH (UNII: 24SC3U704I)
RETINYL PALMITATE (UNII: 1D1K0N0VVC)
BEHENYL ALCOHOL (UNII: 9G1OE216XY)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
ETHYLHEXYL COCOATE (UNII: I1MPW273QS)
COCOGLYCERIDES (UNII: ISE9I7DNUG)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALCOHOL (UNII: 3K9958V90M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ISOAMYL LAURATE (UNII: M1SLX00M3M)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ORYZA SATIVA (RICE) STARCH (UNII: 4DGK8B7I3S)
DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10356-580-05	1 in 1 CARTON	11/26/2024
1		50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/26/2024

Labeler - Beiersdorf Inc (001177906)